Tabs Group | Vectors (Formerly: SP Tabs group)

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1. Introduction

2. XSD schema files

XML file format

1. Introduction

WMDA is using XML (Extensible Markup Language) file, which is considered an industry standard that is extendable, robust and easy to use. Several people from the community formed a working group to create the required XML Schema Definition (XSD) files. These files define the elements that are allowed in the XML file, the order of the elements and the values that will be accepted. The names of the elements are based upon EMDIS specifications and aligns with the EMDIS Data Dictionary when appropriate. Several elements are basic elements that should be included in all files, but there are also elements that are specific for only donors or only cord blood units (CBUs).

We will now explain the composition of the XML file and how you should use the XSD reference files.

2. XSD schema files

WMDA is offering two XSD schema files that define the structure of your XML file: basicTypes.xsd and Inventories.xsd.

The Inventories file describes the structure of the XML file and the order of the elements. Here you can also find if a certain field is mandatory or not (minOccurs="0"-> not mandatory). This file includes many "complexTypes": an XML element that contains other elements and/or attributes. In the file you can see that the values of the elements can be defined here, like the elements GRID and ID, or that after the name of the field a "type" is defined. For example for the element with name BIRTH_DATE you see type="bareDateType". The definition of "bareDateType" is described in the basicTypes.xsd file.

Related to XSD versions, our data upload system always supports latest 3 versions of XSD. And in this page, we keep the latest version to be displayed. If there is another version, it will be in the collapse object before the tables.

Supported versions now: 2.2, 2.3.
The XSD schema can be download here:

XML schema files version 2.2

XML schema files version 2.3

We will now describe the global structure of the XML file and the elements.

Please note: For a lot of elements, we use abbreviations as allowed values. The explanation of all those abbreviations can be found in the XSD files. Most abbreviations are also the same as used for EMDIS and clarified in the EMDIS dictionary.

2.1 InventoryType elements

Field Identifier	Required	Description	Type	Length	Comment
CREATION_TIME	Yes	Creation time stamp of the inventories (in UTC)	dateTime	minimal 20	Without fractional seconds the length is 20, for example: 2016-08-23T13:16:48Z. Additional notes: CREATION_TIME is defined as "Creation time stamp of the <INVENTORIES>" that means the time in UTC when the complete and valid file was finally created at the registry. This can be the same as SNAPSHOT_TIME.
LISTING_ORGANIZATION	Yes	Organisation that lists the donor/cbu provided as ION	ionType: number between 1000 and 9999	4	Issuing Organisation Number (ION) allocated by ICBBA. This can be different from the POOL when another organisation is sending the data to WMDA.
POOL	Yes	Physical location of the donors/CBUs of the inventory provided as ION	ionType: number between 1000 and 9999	4	Physical location of the donors/CBUs of the inventory provided as ION.
CONTENT_TYPE	Yes	Type of the inventory items, i.e. donor ("D") or CBU ("C")	contentTypeType	1	The content-type is also shown in the fileName. When CONTENT_TYPE is "D", the INVENTORY must contain <DONOR>-blocks. When CONTENT_TYPE is "C", the INVENTORY must contain <CBU>-blocks.
UPDATE_MODE	Yes	Update mode of the inventory, i.e. FULL or DIFF	updateModeType	4	Both UPDATE_MODE of "FULL" and "DIFF" are supported. For "FULL", the complete inventory should be sent without deleted inventory, for "DIFF", only the new, edited, deleted inventory need be sent.
SNAPSHOT_TIME	No	Timestamp of the 'data snapshot' (in UTC)	dateTime	minimal 20	Without fractional seconds the length is 20, for example: 2016-08-23T13:16:48Z Additional notes: SNAPSHOT_TIME in the element <INVENTORY> is defined as "timestamp of the data snapshot in UTC" that means the timestamp of the creation of this part of the complete file. This can be the timestamp of the XML export and I guess that in most of the cases it will be identical to the CREATION_TIME.
SCHEMA_VERSION	Yes	Version of the applied XML Schema Definition (XSD)	schemaVersionType		The schema version is very important as this determines the validation rules that should be applied during the processing of your file.

2.2 ItemBaseType elements (for Donors and CBUs)

Expand

title	XSD 2.1

Field Identifier

Required

Description

Type

Length

Comment

ID

No for Donor

Yes for CBU

Unique identifier of the donor/CBU

String

17

Unique identifier of the donor/CBU:

If you are an EMDIS member, you can use the same ID as you use for that system (EMDIS hub code + donor identification allocated by the associated donor registry).

For non-EMDIS members we recommend to use two digit ISO country code of the associated donor registry + donor identification allocated by the associated donor registry. For example: AU600196166, DEGOE-35487, US087013165, SB45.

However, you are also allowed to use just the donor ID allocated by your registry.

Expand

title	XSD 2.2

Field Identifier

Required

Description

Type

Length

Comment

ID

No for Donor

Yes for CBU

Unique identifier of the donor/CBU

String

25

Unique identifier of the donor/CBU:

If you are an EMDIS member, you can use the same ID as you use for that system (EMDIS hub code + donor identification allocated by the associated donor registry).

For non-EMDIS members we recommend to use two digit ISO country code of the associated donor registry + donor identification allocated by the associated donor registry. For example: AU600196166, DEGOE-35487, US087013165, SB45.

However, you are also allowed to use just the donor ID allocated by your registry.

Update from XSD 2.2

GRID

Yes for Donor

No for CBU

Global registration identifier of the donor

String

19

ONLY applicable for donors. GRID format allowed is: XXXXXXXXXXXXXXXXXXX. Only upper case letter and numbers are allowed. The first 4 characters include the ION were the donor is registered. The following 13 characters contain the donor specific ID and the last two characters are check characters that are calculated from the 17 previous characters.

Note: For the generation of the value of GRID, check the "checksum" calculation rule in GRID user guide and a WMDA "checksum" calculator example here.

Field Identifier	Required	Description	Type	Length	Comment
ATTR	No	Describing attribute of the donor/CBU according to house rules of the sending organization.	String	3
BIRTH_DATE	Yes	Date of birth of the donor/CBU	bareDateType	10	Date without timezone information, example 1968-06-28, Date Delimiter = "-"
SEX	No	Biological gender of the donor/CBU	sexType	1	sexType: "F","M" F = Female M = Male NOTE: Mandatory for donors, optional for CBUs
ABO	No	Blood group (ABO) of the donor/CBU	aboType	2	aboType: "A","B","O","AB"
RHESUS	No	Rhesus (Rh) factor of the donor/CBU	rhesusType	1	rhesusType: "P","N" P = Positive N = Negative NOTE: "+" and "-" are not supported
ETHN	No	Ethnic group of the donor/CBU	ethnType	4	ethnType: "AFNA","AFSS", "ASSW", "ASSO", "ASCE", "ASSE", "ASNE", "ASOC", "CAEU", "CAER", "CANA", "CAAU", "HICA", "HISA", "AF", "AS", "CA", "HI", "MX", "OT","UK" AFNA = African: North Africa AFSS = African: Sub-Sahara Africa ASSW = Asian: Southwest Asia (Middle East, Turkey) ASSO = Asian: Southern Asia (India, Pakistan, Bangladesh, Sri Lanka, Bhutan, Nepal) ASCE = Asian: Central Asia (Eastern Russia, Kazakhstan, Uzbekistan, Kyrgyzstan, Tajikistan) ASSE = Asian: Southeast Asia (China, Mongolia, Burma, Laos, Cambodia, Thailand, Vietnam, Taiwan) ASNE = Asian: North and Northeast Asia (Japan, North Korea, South Korea) ASOC = Asian: Oceania (Pacific Islands, excluding Japan, Australia, Taiwan, Sakhalin, Aleutian Islands) CAEU = Caucasian: Mainland Europe, Greenland, Iceland, Western Russia CAER = Caucasian: Eastern Russia CANA = Caucasian: North America (USA, Canada, Mexico) CAAU = Caucasian: Australia (Australia, New Zealand) HICA = Hispanic: Central America, Caribbean HISA = Hispanic: South America MX = Mixed / multiple OT = Other (e.g. Australian Aborigine) UK = Unknown
CCR5	No	CCR5 status of the donor/CBU	ccr5Type	2	ccr5Type: "DD","WW","DW" DD = Deletion (delta 32) - homozygous DW = Deletion (delta 32) / wildtype - heterozygous WW = Wildtype - homozygous
HLA	Yes	HLA of the donor/cbu	hlaType		Explained separately at hlaType 2.3
KIR	No	KIR genotype of the donor/CBU	kirType		Explained separately at kirType 2.4
IDM	No	Infectious disease markers (IDM) and other relevant tests of the donor/CBU	idmType		Explained separately at idmType 2.5
RSV_PAT	No	Unique identifier of the patient the donor/CBU is reserved for (STATUS=RS).	String	17	The value comprises the EMDIS patient identification, where the patient search centre is an EMDIS member, otherwise the value is empty. For example: AU9654021, DE275342, US2277450. NOTE: This field is not required for status "RS" and can be transmitted as empty if privacy concerns exist.
STATUS	Yes	Status of the donor/CBU	statusType	2	statusType: "AV" ,"TU" ,"RS" , "DE" ( "DE" is not supported in "FULL" mode, and supported in "DIFF" mode) AV = Available for transplantation purposes TU = Temporarily unavailable RS = Reserved DE = Deleted, permanently unavailable
STAT_END_DATE	No	Date until which the current status will be applicable	bareDateType	10	Date without timezone information, example 1968-06-28, Date Delimiter = "-"

2.3 hlaType elements

HlaType fields can be divided in hlaSerFieldsType and hlaDnaFieldsType

hlaSerFieldsType: HLA values obtained by serological typing methods

hlaSerFieldsType = “<FIELD1>” string of max length 5 “</FIELD1>”, “<FIELD2>” string of max length 5 “</FIELD2>”;

Example: <SER><FIELD1>1</FIELD1><FIELD2>5</FIELD2></SER>

Serological typing results can be given for loci that are defined as hlaLocusSerDnaType. These loci include HLA-A, -B, -C, -DRB1, -DQB1.

hlaDnaFieldsType: HLA values obtained by DNA based typing methods

hlaDnaFieldsType = “<FIELD1>” string of max length 20 “</FIELD1>”, “<FIELD2>” string of max length 20 “</FIELD2>”;

Example: <DNA><FIELD1>01:01</FIELD1><FIELD2>05:01</FIELD2></DNA>

DNA typing results can be given for loci that are defined as hlaLocusSerDnaType and hlaLocusDnaOnlyType. These loci include HLA-A, -B, -C, -DRB1, -DQB1, -DRB3, -DRB4, -DRB5, -DQA1, -DPA1, -DPB1.

Finally, previously the dot20 file format allowed to submit values like 01 in DNA fields. We can no longer accept this and you have to submit the equivalent of 01, so '01:XX' .

hlaGlsFieldType: HLA GL String typing value or GL String like typing value.

hlaGlsFieldType = "<GLS>"string of max length 255"</GLS>"

Example: <GLS>008:01:01/008:01:02/008:03/008:04+018:01/018:02</GLS>

DNA GL String like typing is now used for MICA and MICB.

Full HLA example:
Please notice the "..." should be filled with the HLA data like in <A>, if no value, the HLA type should be excluded, or include without "...".

Minimal required elements

Minimal typing values for Donor: A (either SER or DNA), B (either SER or DNA)

Minimal typing values for CBU: A (either SER or DNA), B (either SER or DNA), DRB1 (either SER or DNA)

Please note:

It is no longer possible to submit string HLA values; only single values are allowed.
When a donor or CBU has homozygous alleles/values, please use the following notation:

or

Field Identifier	Required	Description	Type	Length	Comment
SER	depends on content type and DNA fields provided	HLA values obtained by serological typing methods	hlaSerFieldsType	5	Each SER element contains two other elements: FIELD1 and FIELD2
DNA	depends on content type and SER fields provided	HLA values obtained by DNA based typing methods	hlaDnaFieldsType	20	Each DNA element contains two other elements: FIELD1 and FIELD2
FIELD1		HLA value of allele 1		5 or 20	Element within the element SER and DNA
FIELD2		HLA value of allele 2		5 or 20	Element within the element SER and DNA
GLS		HLA typing result provided as GL String	hlaGlsFieldType	255	GLS element contains the HLA typingresult in GL String
A	Yes	HLA-A values	hlaLocusSerDnaType		Both SER and DNA possible; either SER or DNA values required
B	Yes	HLA-B values	hlaLocusSerDnaType		Both SER and DNA possible; either SER or DNA values required
C	No	HLA-C values	hlaLocusSerDnaType		Both SER and DNA possible
E	No	HLA-E values	hlaLocusDnaOnlyType	20	Only DNA possible
DRB1	Yes (CBU) No (Donor)	HLA-DRB1 values	hlaLocusSerDnaType	5 or 20	Both SER and DNA possible; either SER or DNA values required for CBU
DRB3	No	HLA-DRB3 values	hlaLocusDnaOnlyType	20	Only DNA possible
DRB4	No	HLA-DRB4 values	hlaLocusDnaOnlyType	20	Only DNA possible
DRB5	No	HLA-DRB5 values	hlaLocusDnaOnlyType	20	Only DNA possible
DQA1	No	HLA-DQA1 values	hlaLocusDnaOnlyType	20	Only DNA possible
DQB1	No	HLA-DQB1 values	hlaLocusSerDnaType	5 or 20	Both SER and DNA possible
DPA1	No	HLA-DPA1 values	hlaLocusDnaOnlyType	20	Only DNA possible
DPB1	No	HLA-DPB1 values	hlaLocusDnaOnlyType	20	Only DNA possible
MICA	No	MHC class I polypeptide-related sequence A	hlaLocusGlsOnlyType	255	GL String like value, example: 008:01:01/008:01:02/008:03/008:04+018:01/018:02
MICB	No	MHC class I polypeptide-related sequence B	hlaLocusGlsOnlyType	255	GL String like value

2.4 kirType elements

The kirType Field Definitions consists of the type: kirLocusType. This is defined as a String with 3 characters: "POS" or "NEG". "POS" means "Presence of KIR gene", "NEG" means "Absence of KIR gene".

The following elements are possible and in this specific order:

<KIR2DL1>,<KIR2DL2>,<KIR2DL3>,<KIR2DL4>,<KIR2DL5A>,<KIR2DL5B>,<KIR2DS1>,<KIR2DS2>,<KIR2DS3>,<KIR2DS4>,<KIR2DS5>,<KIR2DP1>,<KIR3DL1>,<KIR3DL2>,<KIR3DL3>,<KIR3DS1>,<KIR3DP1>.

Expand

title	XSD 2.1, XSD 2.2

Field Identifier	Required	Description	Type	Length	Comment
KIR_GL	No	URI that refers to a GL String registered with a GL service or direct GL String for absence / presence	string	255	This field is not used at the moment and must be empty.

Field Identifier	Required	Description	Type	Length	Comment
KIR gene e.g. KIR2DL1	No	KIR genotype e.g. KIR gene 2DL1	kirLocusType	3	valid values: "POS" = presence of KIR gene; "NEG" = absence of KIR gene
KIR_GL_URI	No	URI that refers to a GL String registered with a GL service or direct GL String for absence / presence	string	255	This field is updated and supported from XSD 2.3

2.5 idmType elements

There are many infectious disease markers (IDM) possible in the element IDM. Many IDM elements can have either the values idmValueType or idmValueExtType

idmValueType includes the following values: "P","N"

idemValueExtType include the following values: “P”,“G”,“M”,“B”,“H”,“O”,“N”

Only when there is old version fields name, then will be in a separated collapse box:

Expand

title	XSD 2.1-Expand to see details

Field Identifier

Required

Description

Type

Length

Comment

CMV

No

Cytomegalovirus status

idmValueExtType

1

idmValueExtType: “P”,“G”,“M”,“B”,“H”,“O”,“N”

P = IgG or IgM positive, test did not differentiate
G = IgG positive, IgM negative
M = IgG negative, IgM positive
B = Both IgG and IgM positive
H = IgG positive, IgM not tested
O = IgG negative, IgM not tested
N = Both IgG and IgM negative

EMDIS data dictionary also has a ‘Q’ (questionable / unclear) but that will not be applicable within the data submission file.

CMV_DATE

No

Date of CMV test

bareDateTyp

10

Date without timezone information, example 1968-06-28, Date Delimiter = "-"

Field Identifier	Required	Description	Type	Length	Comment
ANTI_CMV	No	Antibody to Cytomegalovirus status	idmValueExtType	1	idmValueExtType: “P”,“G”,“M”,“B”,“H”,“O”,“N” P = IgG or IgM positive, test did not differentiate G = IgG positive, IgM negative M = IgG negative, IgM positive B = Both IgG and IgM positive H = IgG positive, IgM not tested O = IgG negative, IgM not tested N = Both IgG and IgM negative EMDIS data dictionary also has a ‘Q’ (questionable / unclear) but that will not be applicable within the data submission file.
CMV_NAT	No	Cytomegalovirus nucleic acid testing (NAT) status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
ANTI_CMV_DATE	No	Date of CMV test	bareDateTyp	10	Date without timezone information, example 1968-06-28, Date Delimiter = "-"
CMV_NAT_DATE	No	Date of CMV NAT test	bareDateTyp	10	Date without timezone information, example 1968-06-28, Date Delimiter = "-"
HBS_AG	No	Hepatitis B status (hepatitis B surface antigen)	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
ANTI_HBC	No	Hepatitis B status (antibody to hepatitis B core antigen)	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
ANTI_HBS	No	Hepatitis B status (antibody to hepatitis B surface antigen)	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
ANTI_HCV	No	Hepatitis C status (antibody to hepatitis C virus)	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
ANTI_HIV_12	No	Antibody to Human immunodeficiency virus (HIV) 1/2 status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
HIV_1_NAT	No	Human immunodeficiency virus (HIV)-1 nucleic acid testing (NAT) status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
HIV_P24	No	Human immunodeficiency virus (HIV) p24 status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
HCV_NAT	No	Hepatitis C nucleic acid testing (NAT) status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
ANTI_HTLV	No	Antibody to human T-cell lymphotropic virus (HTLV) I/II status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
SYPHILIS	No	Syphilis status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
WNV	No	West Nile Virus status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
CHAGAS	No	Chagas status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
EBV	No	Epstein Barr Virus status	idmValueExtType	1	idmValueExtType: “P”,“G”,“M”,“B”,“H”,“O”,“N” P = IgG or IgM positive, test did not differentiate G = IgG positive, IgM negative M = IgG negative, IgM positive B = Both IgG and IgM positive H = IgG positive, IgM not tested O = IgG negative, IgM not tested N = Both IgG and IgM negative EMDIS data dictionary also has a ‘Q’ (questionable / unclear) but that will not be applicable within the data submission file. Please leave blank for Q.
TOXO	No	Toxoplasmosis status	idmValueExtType	1	idmValueExtType: “P”,“G”,“M”,“B”,“H”,“O”,“N” P = IgG or IgM positive, test did not differentiate G = IgG positive, IgM negative M = IgG negative, IgM positive B = Both IgG and IgM positive H = IgG positive, IgM not tested O = IgG negative, IgM not tested N = Both IgG and IgM negative EMDIS data dictionary also has a ‘Q’ (questionable / unclear) but that will not be applicable within the data submission file. Please leave blank for Q.
HBV_NAT	No	Hepatitis B virus (HBV) nucleic acid testing (NAT) status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
PB19_NAT	No	ParvoB19 nucleic acid testing (NAT) status	idmValueType	1	idmValueType: "P","N" P = Positive N = Negative
ALT	No	Alanine aminotransferase status in units per litre	Short		Number, no decimals, minimal value is 1

2.6 donItemType elements

DonItemType elements contain elements that are specific for donors and not applicable for CBUs.

Field Identifier	Required	Description	Type	Length	Comment
ID	No	Unique identifier of the donor	String	25	Same field name used for unique identifier of the donor/CBU: If you are an EMDIS member, you can use the same ID as you use for that system (EMDIS hub code + donor identification allocated by the associated donor registry). For non-EMDIS members we recommend to use two digit ISO country code of the associated donor registry + donor identification allocated by the associated donor registry. For example: AU600196166, DEGOE-35487, US087013165, SB45. However, you are also allowed to use just the donor ID allocated by your registry.
GRID	Yes	Global registration identifier of the donor	String	19	ONLY applicable for donors. GRID format allowed is: XXXXXXXXXXXXXXXXXXX. Only upper case letter and numbers are allowed. The first 4 characters include the ION were the donor is registered. The following 13 characters contain the donor specific ID and the last two characters are check characters that are calculated from the 17 previous characters. Note: For the generation of the value of GRID, check the "checksum" calculation rule in GRID user guide and a WMDA "checksum" calculator example here. More detail you can check the GRID project page here.
STAT_REASON	No	Additional information relevant to the donor status. Can only be used for "TU" status.	statReasonDonType	2	statReasonDonType: "DO", "DD","MR", "PR","TX", "MO", "UC", "OT", "TQ", "UK" DO = Donor is too old DD = Donor died MR = Medical reasons PR = Personal reasons TX = After transplantation MO = Donor has moved UC = Unable to contact donor OT = Other reasons TQ = Typing questionable UK = Unknown
CONTACT_DATE	No	Date of last confirmed contact - defined as the date of an active form of communication (e.g. a query about status, an address update, confirmation of their interest in donating) via any channel (e.g. email, mail, phone, website), post registration, from a donor to the registry. Any communication from the registry to the donor that does not lead to an activity of the donor suggesting his further interest in donation is explicitly excluded (e.g. annual mailing without reaction).	bareDateType	10	Date without timezone information, example 1968-06-28, Date Delimiter = "-"
CHECKUP_DATE	No	Date of the last medical checkup - defined as the date of a donor health assessment that indicates whether a donor is minimally suitable to be considered for donation, regardless if eligible for only one donation type, and includes questions about current medication and health issues (e.g. completion of a health screening questionnaire at Extended Typing or Verification Typing). The donor health assessment can be completed by any means (e.g. paper-based, online, phone). This does not require any physical examination of a donor.	bareDateType	10	Date without timezone information, example 1968-06-28, Date Delimiter = "-"
WEIGHT	No	Weight in kg Please note that current validation only allows [40-199] kg	Short		Number between 1 and 999, no decimals
HEIGHT	No	Height in cm Please note that current validation only allows [100-250] cm	Short		Number between 1 and 999, no decimals
NMBR_TRANS	No	Number of blood transfusions	Short		Number: zero or greater, no decimals
NMBR_PREG	No	Number of pregnancies	Short		Number: zero or greater, no decimals
NMBR_MARR	No	Number of marrow donations	Short		Number: zero or greater, no decimals
NMBR_PBSC	No	Number of PBSC donations	Short		Number: zero or greater, no decimals
COLL_TYPE	No	Collection type, i.e. the willingness of the donor to donate in a specific manner	String	1	collTypeType: "M", "P","B" M = Marrow P = PBSC B = Both PBSC & Marrow

2.7 cbuItemType elements

CbuItemType elements contain elements that are specific for CBUs and not applicable for donors.

Field Identifier

Required

Description

Type

Length

Comment

ID

Yes

Unique identifier of the CBU

String

25

Same field name used for unique identifier of the donor/CBU::

If you are an EMDIS member, you can use the same ID as you use for that system (EMDIS hub code + donor identification allocated by the associated donor registry).

For non-EMDIS members we recommend to use two digit ISO country code of the associated donor registry + donor identification allocated by the associated donor registry. For example: AU600196166, DEGOE-35487, US087013165, SB45.

However, you are also allowed to use just the donor ID allocated by your registry.

STAT_REASON

No

Additional information relevant to the CBU status. Can only be used for "TU" status.

statReasonCbuType

2

statReasonCbuType: "QR","AD","CD","DS","XP","MR","OT","UK"

Proposed reasons for Status TU:
QR = Quarantined;
AD = Administrative

Proposed reasons for Status DE:
CD = Cord Destroyed or Damaged;
DS = Distributed for infusion;
XP = ExpiredCD = Cord Destroyed or Damaged;
MR = Medical reasons
OT = Unavailable for other reasons;
UK = Unknown

LOCAL_ID

No

Identification of CBU locally at the associated CBB

String

17

BAG_ID

No

Identification as it appears on the bag. If more than one bag is available then this data attribute is not populated

String

17

BANK_MANUF_ID

No

Unique identifier of the CBB that manufactured the CBU. ID shown in table in tab Cord blood bank IDs

String

10

PLEASE NOTE: For the upload the fields BANK_MANUF_ID and BANK_DISTRIB_ID should be fulfilled with a new ID in WMDA attribute for the corresponding cord blood banks (See column "WO number at share.wmda.info/display/WMDAREG/Database ) and EMDIS IDs can be filled in the EMDIS attribute.

These IDs in WMDA attribute are important to allow WMDA to identify if the CBU is from an accredited bank which will be displayed within a search report. The supported accreditation are FACT, AABB, WMDA C/D accreditation.

Example of the valid XML format:

Code Block

language	xml
title	BANK_MANUF_ID XML example

<BANK_MANUF_ID WMDA="3847" EMDIS="EN-38" />
<BANK_MANUF_ID EMDIS="EN-38" />
<BANK_MANUF_ID WMDA="3847" />
<BANK_MANUF_ID WMDA="3847" EMDIS="EN-38"></BANK_MANUF_ID>
<BANK_MANUF_ID></BANK_MANUF_ID>
<BANK_MANUF_ID />

Last update in XSD 2.2

BANK_DISTRIB_ID

No

Unique identifier of the CBB distributing the CBU. ID shown in table in tab Cord blood bank IDs

String

10

PLEASE NOTE: For the upload the fields BANK_MANUF_ID and BANK_DISTRIB_ID should be fulfilled with a new ID in WMDA attribute for the corresponding cord blood banks (See column "WO number at share.wmda.info/display/WMDAREG/Database ) and EMDIS IDs can be filled in the EMDIS attribute.

These IDs in WMDA attribute are important to allow WMDA to identify if the CBU is from an accredited bank which will be displayed within a search report. The supported accreditation are FACT, AABB, WMDA C/D accreditation.

Example of the valid XML format:

Code Block

language	xml
title	BANK_MANUF_ID XML example

<BANK_DISTRIB_ID WMDA="3847" EMDIS="EN-38" />
<BANK_DISTRIB_ID EMDIS="EN-38" />
<BANK_DISTRIB_ID WMDA="3847" />
<BANK_DISTRIB_ID WMDA="3847" EMDIS="EN-38"></BANK_DISTRIB_ID>
<BANK_DISTRIB_ID></BANK_DISTRIB_ID>
<BANK_DISTRIB_ID />

Last update in XSD 2.2

COLL_DATE

No

Date that the CBU was collected

bareDateType

10

Date without timezone information, example 1968-06-28, Date Delimiter = "-"

PROC_DATE

No

Date that the processing started

bareDateType

10

Date without timezone information, example 1968-06-28, Date Delimiter = "-"

PROC_METH

No

Processing method used

procMethType

3

procMethType: "HES","DGS","CEN","FIL","FIC","PER","OTH"

HES = Hydroxy-Ethyl-Starch
DGS = Density Gradient Separation
CEN = Centrifuge
FIL = Filtration
FIC = FICOL
PER = PERCOL
OTH = Other

NOTE: Values "NOT" and "UNK" are not supported

"NOT" can now be found in CB_PROD_MOD = "NOT", "UNK" has to be transmitted as empty (CB_PROD_MOD = "")

PROC_METH_TYPE

No

Processing method type used

procMethTypeType

3

procMethTypeType: "MAN","SPX","OTP","AXP","OTH"

MAN = Manual
SPX = Sepax
OTP = Optipress II
AXP = AXP
OTH = Other

FREEZE_DATE

No

Date that the CBU was frozen

bareDateType

10

Date without timezone information, example 1968-06-28, Date Delimiter = "-"

FREEZE_METH

No

Freezing method used

freezeMethType

1

freezeMethType: "C","M"

C = Controlled Rate
M = Manual

PROD_MOD

No

Product modifications made

prodModType

3

prodModType: "BCE","DNE","PLR","PRR","RBR","NOT","OTH"

BCE = Buffy Coat Enriched
DNE = Density Enriched
PLR = Plasma Reduced (Volume reduction only)
PRR = Plasma and RBC Reduced
RBR = RBC Reduced (depletion)
NOT = Not reduced
OTH = Other

BAG_TYPE

No

Type of bag used (bag fractions / split unit)

bbagTypeType

5

bagTypeType: "80/20","50/50","40/60","NS" (no split)

BAGS

No

Number of bags for CBU sub units

Short

Number between 1 and 99, no decimals

BACT_CULT

No

Bacterial culture

cultValueType

1

cultValueType: "P","N","D"

P = Positive N = Negative D = Not done

FUNG_CULT

No

Fungal culture

cultValueType

1

cultValueType: "P","N","D"

P = Positive N = Negative D = Not done

HEMO_STATUS

No

Hemoglobinopathy screening status

hemoStatusType

2

hemoStatusType: "DN","DU","NS","CD","NC","DT","DD"

DN = Screening done, normal results
DU = Screening done, unusual findings
NS = No screening done
CD = Can be done at time of release
NC = Cannot be done
DT = Thalassemia
DD = Drepanocytosis

VOL

No

Collected volume before processing (without additives) in ml

Short

Number between 10 and 400, no decimals

VOL_FRZN

No

Total volume frozen (post processing, prior to cryopreservation) in ml

Short

Number between 10 and 400, no decimals

TNC

No

Total number of nucleated cells (before processing)

Float

Number with decimals, minimum is 0.0E0, maximum is 999.9E7

TNC_FRZN

No

Total number of nucleated cells (post processing, prior to cryopreservation)

Float

Number with decimals, minimum is 0.0E0, maximum is 999.9E7

RED_BC_FRZN

No

Total number of nucleated red blood cells (post processing, prior to cryopreservation)

Float

Number with decimals: minimum is 0.0E0, maximum is 999.9E7

MNC_FRZN

No

Total Number of mononucleated cells (post processing, prior to cryopreservation)

Float

Number with decimals

CD34PC

No

Total number of CD34+ cells (before processing)

Float

Number with decimals

CD34PC_FRZN

No

Total number of CD34+ cells (post processing, prior to cryopreservation)

Float

Number with decimals

CFU_FRZN

No

Total count of colony forming units (post processing, prior to cryopreservation)

Float

Number with decimals, nunimum is 0.1E5, maxnum is 999.9E5

VIABILITY

No

Viability as percentage value

Short

Number between 0 and 100, no decimals

VIABILITY_DATE

No

Date that viability was tested

bareDateType

10

Date without timezone information, example 1968-06-28, Date Delimiter = "-"

VIABILITY_CELLS

No

Type of cells tested for viability

viabilityCellsType

6

viabilityCellsType: "TNC","CD34PC","CD45PC"

NOTE:

VIABILITY_CELLS = "CD34PC" corresponds to CB_VIABILITY_CELLS = "CD34" in EMDIScord.

VIABILITY_CELLS = "CD45PC" corresponds to CB_VIABILITY_CELLS = "CD45" in EMDIScord.

VIABILITY_METHOD

No

Method used to calculate the viability

viabilityMethodType

2

viabilityMethodType: "7A","PI","TB","OT"

7A = 7AAD
PI = Propidium Iodide
TB = Trypan Blue
OT = Other

ATT_SEG

No

Number of attached segments available

Short

Number between 0 and 99, no decimals

DNA_SMPL

No

DNA samples available?

Boolean

true,false

OTH_SMPL

No

Samples other than DNA available?

Boolean

true,false

CT_COMPLETE_DATE

No

Date of completion of confirmatory typing (CT)

bareDateType

10

Date without timezone information, example 1968-06-28, Date Delimiter = "-"

CT_SMPL_TYPE

No

Confirmatory typing (CT) sample type

ctSmplTypeType

2

ctSmplTypeType: "AS","WB","RC","FP","ED"

AS = CBU Contiguous Attached Segment
WB = Whole Blood Sample
RC = Red Cell Fraction (pellet)
FP = Blood Spotted Filter Paper
ED = Extracted DNA

AL_RED_BC

No

Number of red cell fraction aliquots

Short

Number between 0 and 99, no decimals

AL_SER

No

Number of serum aliquots available

Short

Number between 0 and 99, no decimals

SER_QUANT

No

Total quantity of serum available in ml

Float

Number between 0.0 and 99.9, one decimal

AL_PLA

No

Number of plasma aliquots available

Short

Number between 0 and 99, no decimals

PLA_QUANT

No

Total quantity of plasma available in ml

Float

Number between 0.0 and 99.9, one decimal

MAT

No

Data of the mother of the infant associated with the CBU

matType

see further on this webpage matType

2.8 matType elements

The matType elements are a sub-element from the element CBU.

Field Identifier	Required	Description	Type	Length	Comment
ID	No	Identification used to identify the maternal donor as assigned by the registry	String	15
ID_BANK	No	Identification used by associated CBU manufacturer to identify maternal detail	String	15
HLA	No	HLA of the mother of the infant associated with the CBU	hlaType		see above in section 2.3 hlaType
IDM	No	Infectious disease markers (IDM) and other relevant tests of the mother of the CBU	idmType		see above in section 2.5 idmType
AL_SER	No	Number of serum aliquots available	short		Number between 0 and 99, no decimals
SER_QUANT	No	Total quantity of serum available in ml	Float		Number between 0.0 and 99.9, one decimal
AL_PLA	No	Number of plasma aliquots available	Short		Number between 0 and 99, no decimals
PLA_QUANT	No	Total quantity of plasma available in ml	Float		Number between 0.0 and 99.9, one decimal

Tab Pane | Vectors (Formerly: SP Tab pane)

anchor	83410132
name	Minimal required data

#

Minimal required data

Organisations providing donor or CBU data, should at least include the following elements with valid values. Without this data, the records will be rejected during the validation procedure.

Note: For For the generation of the value of GRID, check the "checksum" calculation rule in GRID user guide and a WMDA "checksum" calculator example here. More detail of the introduction and "checksum" calculation rule, you can check the GRID project page ISBT 128 Standard for GRID here.

A DONOR record should include:

GRID
BIRTH_DATE
SEX
HLA (including at least HLA-A (SER or DNA) and HLA-B (SER or DNA))
STATUS

A CBU record should include:

ID
BIRTH_DATE
HLA (including at least HLA-A (SER or DNA), HLA-B (SER or DNA) and HLA-DRB1 (SER or DNA))
STATUS

Tab Pane | Vectors (Formerly: SP Tab pane)

anchor	273469870
name	XML examples

#

XML example files

We already provided you the XSD files, but these files do not show directly how an XML file with those definitions will look like. Therefore we created some example files: one for donors and one for CBUs.

The XSD schema can be download here:

XML schema files version 2.2

XML schema files version 2.3

Both files contain only 2 records, but in those two records almost all possible elements contain a value. It can help you to check the order of the elements in your own XML file. Please be aware that values like GRID are fictive and do not follow the rules for the check character.

We suggestion you to always implement the latest version.

Important to know for XML structure:

Currently, the error handling can not handle the data structure as below if there is no records included for both FULL/DIFF upload mode.

Code Block

language	xml
title	Not Accepted XML structure

<?xml version='1.0' encoding='UTF-8'?>
<INVENTORIES CREATION_TIME="2022-07-01T08:54:00Z">
	<INVENTORY LISTING_ORGANIZATION="1234" POOL="1234" CONTENT_TYPE="D" UPDATE_MODE="FULL" SNAPSHOT_TIME="2021-11-22T08:54:00Z" SCHEMA_VERSION="2.2"/>
</INVENTORIES>

If the upload is for DIFF and there is indeed no record, the format should be as below:

Code Block

language	xml
title	Not Accepted XML structure

<?xml version='1.0' encoding='UTF-8'?>
<INVENTORIES CREATION_TIME="2022-07-01T08:54:00Z">
</INVENTORIES>

XSD 2.3 examples: (Expire in 2024, Q4)

Example donor file: ION-1234-D-XSD23.xml

Code Block

language	xml
title	Example Donor file XSD 2.3
linenumbers	true
collapse	true

<?xml version="1.0" encoding="UTF-8"?>
<INVENTORIES CREATION_TIME="2020-09-05T21:00:03Z">
 <INVENTORY LISTING_ORGANIZATION="1234" POOL="1234" CONTENT_TYPE="D" UPDATE_MODE="FULL" SNAPSHOT_TIME="2020-09-05T22:00:08Z" SCHEMA_VERSION="2.3">
  <DONOR>
   <BIRTH_DATE>1962-02-10</BIRTH_DATE>
   <SEX>F</SEX>
   <ABO>O</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>CA</ETHN>
   <CCR5>DW</CCR5>
   <HLA>
    <A>
      <SER>
      <FIELD1>2</FIELD1>
      <FIELD2>11</FIELD2>
      </SER>
     <DNA>
      <FIELD1>02:CSAH</FIELD1>
      <FIELD2>11:MP</FIELD2>
     </DNA>
    </A>
    <B>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>39</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:XX</FIELD1>
      <FIELD2>39:KBY</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2></FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:HBA</FIELD1>
      <FIELD2>12:CF</FIELD2>
     </DNA>
    </C>
	<E>
	  <DNA>
		<FIELD1>04:01</FIELD1>
		<FIELD2>07:02</FIELD2>
	  </DNA>
	</E>
    <DRB1>
    <SER>
      <FIELD1>12</FIELD1>
      <FIELD2>15</FIELD2>
      </SER>
     <DNA>
      <FIELD1>12:GS</FIELD1>
      <FIELD2>15:CCZ</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5>
    <DNA>
    <FIELD1>01:01</FIELD1>
    <FIELD2></FIELD2>
    </DNA>
    </DRB5>
    <DQA1></DQA1>
    <DQB1>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>6</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:01</FIELD1>
      <FIELD2>06:02</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
     <DNA>
      <FIELD1>04:01</FIELD1>
      <FIELD2>03:01</FIELD2>
     </DNA>
    </DPB1>
	<MICA>
        <GLS>008:01:01/008:01:02/008:03/008:04+018:01/018:02</GLS>
    </MICA>
	<MICB>
        <GLS>003/005:02:01/005:02:02/005:02:03/005:02:04/005:08/006/010+003/005:02:01/005:02:02/005:02:03/005:02:04/005:08/006/010</GLS>
    </MICB>
   </HLA>
   <KIR>
    <KIR2DL1>NEG</KIR2DL1>
    <KIR2DL2>POS</KIR2DL2>
    <KIR2DL3>NEG</KIR2DL3>
    <KIR2DL4>NEG</KIR2DL4>
    <KIR2DL5A>NEG</KIR2DL5A>
    <KIR2DL5B>NEG</KIR2DL5B>
    <KIR2DS1>POS</KIR2DS1>
    <KIR2DS2>NEG</KIR2DS2>
    <KIR2DS3>NEG</KIR2DS3>
    <KIR2DS4>NEG</KIR2DS4>
    <KIR2DS5>NEG</KIR2DS5>
    <KIR2DP1>NEG</KIR2DP1>
    <KIR3DL1>NEG</KIR3DL1>
    <KIR3DL2>NEG</KIR3DL2>
    <KIR3DL3>NEG</KIR3DL3>
    <KIR3DS1>NEG</KIR3DS1>
    <KIR3DP1>NEG</KIR3DP1>
	<KIR_GLS_URI>https://gl.nmdp.org/nonstrict/multilocus-unphased-genotype/4p</KIR_GLS_URI>
   </KIR>
   <IDM>
	<ANTI_CMV>H</ANTI_CMV>
	<ANTI_CMV_DATE>2016-06-24</ANTI_CMV_DATE>
	<CMV_NAT>P</CMV_NAT>
	<CMV_NAT_DATE>2016-06-24</CMV_NAT_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>1</ALT>
   </IDM>
   <RSV_PAT>ABCD1234567</RSV_PAT>
   <STATUS>RS</STATUS>
   <STAT_END_DATE>2022-10-20</STAT_END_DATE>
   <ID>WMDA001</ID>
   <GRID>1234000000WMDA00121</GRID>
   <STAT_REASON>TX</STAT_REASON>
   <CONTACT_DATE>2016-12-15</CONTACT_DATE>
   <WEIGHT>65</WEIGHT>
   <HEIGHT>175</HEIGHT>
   <NMBR_TRANS>1</NMBR_TRANS>
   <NMBR_PREG>1</NMBR_PREG>
   <NMBR_MARR>0</NMBR_MARR>
   <NMBR_PBSC>0</NMBR_PBSC>
   <COLL_TYPE>B</COLL_TYPE>
  </DONOR>
  <DONOR>
   <BIRTH_DATE>1960-04-22</BIRTH_DATE>
   <SEX>M</SEX>
   <ABO>A</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>CA</ETHN>
   <CCR5>DD</CCR5>
   <HLA>
    <A>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>24</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:VJKM</FIELD1>
      <FIELD2>24:EJPF</FIELD2>
     </DNA>
    </A>
    <B>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>44</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:BCAU</FIELD1>
      <FIELD2>44:BCXE</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2></FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:ATGS</FIELD1>
      <FIELD2>16:01</FIELD2>
     </DNA>
    </C>
    <DRB1>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>15</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:DWH</FIELD1>
      <FIELD2>15:BMEG</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2></FIELD2>
     </DNA>
     </DRB5>
    <DQA1></DQA1>
    <DQB1>
    <SER>
      <FIELD1>2</FIELD1>
      <FIELD2>6</FIELD2>
      </SER>
     <DNA>
      <FIELD1>02:01</FIELD1>
      <FIELD2>06:02</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
     <DNA>
      <FIELD1>02:02</FIELD1>
      <FIELD2>03:01</FIELD2>
     </DNA>
    </DPB1>
   </HLA>
   <KIR>
   </KIR>
   <IDM>
	<ANTI_CMV>O</ANTI_CMV>
	<ANTI_CMV_DATE>2015-10-20</ANTI_CMV_DATE>
	<CMV_NAT>N</CMV_NAT>
	<CMV_NAT_DATE>2015-10-20</CMV_NAT_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>2</ALT>
   </IDM>
   <STATUS>AV</STATUS>
   <GRID>1234000000WMDA00219</GRID>
   <CONTACT_DATE>2015-10-20</CONTACT_DATE>
   <CHECKUP_DATE>2015-10-20</CHECKUP_DATE>
   <WEIGHT>86</WEIGHT>
   <HEIGHT>187</HEIGHT>
   <NMBR_TRANS>0</NMBR_TRANS>
   <NMBR_MARR>0</NMBR_MARR>
   <NMBR_PBSC>1</NMBR_PBSC>
   <COLL_TYPE>B</COLL_TYPE>
  </DONOR>
 </INVENTORY>
</INVENTORIES>

Example CBU file: ION-1234-C-XSD23.xml

Code Block

language	xml
title	Example CBU file XSD 2.3
linenumbers	true
collapse	true

<?xml version="1.0" encoding="UTF-8"?>
<INVENTORIES CREATION_TIME="2020-09-05T21:00:04Z">
 <INVENTORY LISTING_ORGANIZATION="1234" POOL="1234" CONTENT_TYPE="C" UPDATE_MODE="FULL" SNAPSHOT_TIME="2020-09-05T22:00:05Z" SCHEMA_VERSION="2.3">
  <CBU>
   <BIRTH_DATE>2009-09-02</BIRTH_DATE>
   <SEX>M</SEX>
   <ABO>A</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>AF</ETHN>
   <CCR5>DD</CCR5>
   <HLA>
    <A>
      <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>3</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:XX</FIELD1>
      <FIELD2>03:XX</FIELD2>
     </DNA>
    </A>
    <B>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>55</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:XX</FIELD1>
      <FIELD2>55:XX</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>7</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:03</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
	<E>
	  <DNA>
		<FIELD1>04:01</FIELD1>
		<FIELD2>07:02</FIELD2>
	  </DNA>
	</E>
    <DRB1>
    <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>15</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>15:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5>
    <DNA>
    <FIELD1>01:01</FIELD1>
    <FIELD2></FIELD2>
    </DNA>
    </DRB5>
    <DQA1></DQA1>
    <DQB1>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:02</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
    <DNA>
    <FIELD1>04:02</FIELD1>
    <FIELD2>11:01</FIELD2>
    </DNA>
    </DPB1>
	<MICA>
        <GLS>008:01:01/008:01:02/008:03/008:04+018:01/018:02</GLS>
    </MICA>
	<MICB>
        <GLS>003/005:02:01/005:02:02/005:02:03/005:02:04/005:08/006/010+003/005:02:01/005:02:02/005:02:03/005:02:04/005:08/006/010</GLS>
    </MICB>
   </HLA>
   <KIR>
    <KIR2DL1>NEG</KIR2DL1>
    <KIR2DL2>NEG</KIR2DL2>
    <KIR2DL3>NEG</KIR2DL3>
    <KIR2DL4>POS</KIR2DL4>
    <KIR2DL5A>NEG</KIR2DL5A>
    <KIR2DL5B>NEG</KIR2DL5B>
    <KIR2DS1>POS</KIR2DS1>
    <KIR2DS2>NEG</KIR2DS2>
    <KIR2DS3>NEG</KIR2DS3>
    <KIR2DS4>NEG</KIR2DS4>
    <KIR2DS5>NEG</KIR2DS5>
    <KIR2DP1>NEG</KIR2DP1>
    <KIR3DL1>NEG</KIR3DL1>
    <KIR3DL2>NEG</KIR3DL2>
    <KIR3DL3>NEG</KIR3DL3>
    <KIR3DS1>NEG</KIR3DS1>
    <KIR3DP1>NEG</KIR3DP1>
	<KIR_GLS_URI>https://gl.nmdp.org/nonstrict/multilocus-unphased-genotype/4p</KIR_GLS_URI>
   </KIR>
   <IDM>
    <ANTI_CMV>N</ANTI_CMV>
    <ANTI_CMV_DATE>2009-09-04</ANTI_CMV_DATE>
    <CMV_NAT>N</CMV_NAT>
    <CMV_NAT_DATE>2009-09-04</CMV_NAT_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>1</ALT>
   </IDM>
   <STATUS>AV</STATUS>
   <ID>WMDA0CBU001</ID>
   <LOCAL_ID>CBB000001</LOCAL_ID>
   <BAG_ID>BAG00BMDW001</BAG_ID>
   <BANK_MANUF_ID WMDA="6789" EMDIS="EN-38"></BANK_MANUF_ID>
   <BANK_DISTRIB_ID WMDA="6789" EMDIS="EN-38"></BANK_DISTRIB_ID>
   <COLL_DATE>2009-09-02</COLL_DATE>
   <PROC_DATE>2009-09-02</PROC_DATE>
   <PROC_METH>HES</PROC_METH>
   <PROC_METH_TYPE>SPX</PROC_METH_TYPE>
   <FREEZE_DATE>2009-09-02</FREEZE_DATE>
   <FREEZE_METH>C</FREEZE_METH>
   <PROD_MOD>PRR</PROD_MOD>
   <BAG_TYPE>80/20</BAG_TYPE>
   <BAGS>1</BAGS>
   <BACT_CULT>N</BACT_CULT>
   <FUNG_CULT>N</FUNG_CULT>
   <HEMO_STATUS>DN</HEMO_STATUS>
   <VOL>100</VOL>
   <VOL_FRZN>25</VOL_FRZN>
   <TNC>1.20E9</TNC>
   <TNC_FRZN>9.90E8</TNC_FRZN>
   <RED_BC_FRZN>9.00E7</RED_BC_FRZN>
   <MNC_FRZN>552999973</MNC_FRZN>
   <CD34PC>1.50E6</CD34PC>
   <CD34PC_FRZN>1.10E6</CD34PC_FRZN>
   <CFU_FRZN>1.23E6</CFU_FRZN>
   <VIABILITY>98</VIABILITY>
   <VIABILITY_DATE>2009-09-02</VIABILITY_DATE>
   <VIABILITY_CELLS>CD34PC</VIABILITY_CELLS>
   <VIABILITY_METHOD>7A</VIABILITY_METHOD>
   <ATT_SEG>2</ATT_SEG>
   <DNA_SMPL>true</DNA_SMPL>
   <OTH_SMPL>true</OTH_SMPL>
   <CT_COMPLETE_DATE>2016-09-22</CT_COMPLETE_DATE>
   <CT_SMPL_TYPE>ED</CT_SMPL_TYPE>
   <AL_RED_BC>3</AL_RED_BC>
   <AL_SER>4</AL_SER>
   <SER_QUANT>10.0</SER_QUANT>
   <AL_PLA>2</AL_PLA>
   <PLA_QUANT>10.0</PLA_QUANT>
   <MAT>
    <ID>123456789</ID>
    <ID_BANK>CBB01</ID_BANK>
    <HLA>
    <A>
      <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>68</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:XX</FIELD1>
      <FIELD2>68:XX</FIELD2>
     </DNA>
    </A>
    <B>
     <DNA>
      <FIELD1>07:XX</FIELD1>
      <FIELD2>39:XX</FIELD2>
     </DNA>
    </B>
    <C>
     <DNA>
      <FIELD1>12:03</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
	<E>
	  <DNA>
		<FIELD1>04:01</FIELD1>
		<FIELD2>07:02</FIELD2>
	  </DNA>
	</E>
    <DRB1>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>13:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5></DRB5>
    <DQA1></DQA1>
    <DQB1>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:03</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
    <DNA>
    <FIELD1>04:02</FIELD1>
    <FIELD2>11:01</FIELD2>
    </DNA>
    </DPB1>
	<MICA>
        <GLS>009:01/049+017</GLS>
    </MICA>
	<MICB>
        <GLS>002:01:01/002:01:02+003/005:02:01/005:02:02/005:02:03/005:02:04/005:08/006/010|018+019</GLS>
    </MICB>
    </HLA>
    <IDM>
     <ANTI_CMV>O</ANTI_CMV>
     <ANTI_CMV_DATE>2009-09-04</ANTI_CMV_DATE>
     <CMV_NAT>N</CMV_NAT>
     <CMV_NAT_DATE>2009-09-04</CMV_NAT_DATE>
     <HBS_AG>N</HBS_AG>
     <ANTI_HBC>N</ANTI_HBC>
     <ANTI_HBS>N</ANTI_HBS>
     <ANTI_HCV>N</ANTI_HCV>
     <ANTI_HIV_12>N</ANTI_HIV_12>
     <HIV_1_NAT>N</HIV_1_NAT>
     <HIV_P24>N</HIV_P24>
     <HCV_NAT>N</HCV_NAT>
     <ANTI_HTLV>N</ANTI_HTLV>
     <SYPHILIS>N</SYPHILIS>
     <WNV>N</WNV>
     <CHAGAS>N</CHAGAS>
     <EBV>G</EBV>
     <TOXO>N</TOXO>
     <HBV_NAT>N</HBV_NAT>
     <PB19_NAT>N</PB19_NAT>
     <ALT>2</ALT>
    </IDM>
    <AL_SER>2</AL_SER>
    <SER_QUANT>10.0</SER_QUANT>
    <AL_PLA>3</AL_PLA>
    <PLA_QUANT>15.0</PLA_QUANT>
   </MAT>
  </CBU>
  <CBU>
   <BIRTH_DATE>2010-07-01</BIRTH_DATE>
   <SEX>F</SEX>
   <ABO>O</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>UK</ETHN>
   <CCR5>WW</CCR5>
   <HLA>
    <A>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>30</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:XX</FIELD1>
      <FIELD2>30:XX</FIELD2>
     </DNA>
    </A>
    <B>
      <SER>
      <FIELD1>8</FIELD1>
      <FIELD2>62</FIELD2>
      </SER>
     <DNA>
      <FIELD1>08:XX</FIELD1>
      <FIELD2>15:01</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>7</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:XX</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
    <DRB1>
    <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>13</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>13:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5></DRB5>
    <DQA1></DQA1>
    <DQB1>
    <SER>
      <FIELD1>5</FIELD1>
      <FIELD2>6</FIELD2>
      </SER>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:XX</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
    <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>04:01</FIELD2>
     </DNA></DPB1>
   </HLA>
   <KIR>
    <KIR2DL1>NEG</KIR2DL1>
    <KIR2DL2>POS</KIR2DL2>
    <KIR2DL3>NEG</KIR2DL3>
    <KIR2DL4>NEG</KIR2DL4>
    <KIR2DL5A>NEG</KIR2DL5A>
    <KIR2DL5B>NEG</KIR2DL5B>
    <KIR2DS1>POS</KIR2DS1>
    <KIR2DS2>NEG</KIR2DS2>
    <KIR2DS3>NEG</KIR2DS3>
    <KIR2DS4>NEG</KIR2DS4>
    <KIR2DS5>NEG</KIR2DS5>
    <KIR2DP1>NEG</KIR2DP1>
    <KIR3DL1>NEG</KIR3DL1>
    <KIR3DL2>NEG</KIR3DL2>
    <KIR3DL3>NEG</KIR3DL3>
    <KIR3DS1>NEG</KIR3DS1>
    <KIR3DP1>NEG</KIR3DP1>
   </KIR>
   <IDM>
    <ANTI_CMV>H</ANTI_CMV>
    <ANTI_CMV_DATE>2010-07-04</ANTI_CMV_DATE>
    <CMV_NAT>P</CMV_NAT>
    <CMV_NAT_DATE>2010-07-04</CMV_NAT_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>2</ALT>
   </IDM>
   <RSV_PAT>HHH0123</RSV_PAT>
   <STATUS>RS</STATUS>
   <STAT_END_DATE>2017-09-05</STAT_END_DATE>
   <STAT_REASON>OT</STAT_REASON>
   <ID>WMDA0CBU002</ID>
   <LOCAL_ID>BMDW0CBU002</LOCAL_ID>
   <BAG_ID>BAG00MDW02</BAG_ID>
   <BANK_MANUF_ID WMDA="4567" EMDIS="EN-38"></BANK_MANUF_ID>
   <BANK_DISTRIB_ID WMDA="4567" EMDIS="EN-38"></BANK_DISTRIB_ID>
   <COLL_DATE>2010-07-01</COLL_DATE>
   <PROC_DATE>2010-07-01</PROC_DATE>
   <PROC_METH>HES</PROC_METH>
   <PROC_METH_TYPE>SPX</PROC_METH_TYPE>
   <FREEZE_DATE>2010-07-01</FREEZE_DATE>
   <FREEZE_METH>M</FREEZE_METH>
   <PROD_MOD>PLR</PROD_MOD>
   <BAG_TYPE>50/50</BAG_TYPE>
   <BAGS>1</BAGS>
   <BACT_CULT>N</BACT_CULT>
   <FUNG_CULT>N</FUNG_CULT>
   <HEMO_STATUS>DN</HEMO_STATUS>
   <VOL>49</VOL>
   <VOL_FRZN>25</VOL_FRZN>
   <TNC>5.71E8</TNC>
   <TNC_FRZN>4.33E8</TNC_FRZN>
   <RED_BC_FRZN>9.00E6</RED_BC_FRZN>
   <MNC_FRZN>340999990</MNC_FRZN>
   <CD34PC>2.0E6</CD34PC>
   <CD34PC_FRZN>1.70E6</CD34PC_FRZN>
   <CFU_FRZN>1.65E6</CFU_FRZN>
   <VIABILITY>97</VIABILITY>
   <VIABILITY_DATE>2010-07-02</VIABILITY_DATE>
   <VIABILITY_CELLS>CD34PC</VIABILITY_CELLS>
   <VIABILITY_METHOD>7A</VIABILITY_METHOD>
   <ATT_SEG>3</ATT_SEG>
   <DNA_SMPL>true</DNA_SMPL>
   <OTH_SMPL>true</OTH_SMPL>
   <CT_COMPLETE_DATE>2012-09-02</CT_COMPLETE_DATE>
   <CT_SMPL_TYPE>ED</CT_SMPL_TYPE>
   <AL_RED_BC>3</AL_RED_BC>
   <AL_SER>4</AL_SER>
   <SER_QUANT>10.0</SER_QUANT>
   <AL_PLA>2</AL_PLA>
   <PLA_QUANT>10.0</PLA_QUANT>
   <MAT>
    <ID>113456789-</ID>
    <ID_BANK>CBB001</ID_BANK>
    <HLA>
    <A>
     <DNA>
      <FIELD1>03:XX</FIELD1>
      <FIELD2>01:XX</FIELD2>
     </DNA>
    </A>
    <B>
      <SER>
      <FIELD1>8</FIELD1>
      <FIELD2>7</FIELD2>
      </SER>
     <DNA>
      <FIELD1>08:XX</FIELD1>
      <FIELD2>07:02</FIELD2>
     </DNA>
    </B>
    <C>
     <DNA>
      <FIELD1>07:02</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
    <DRB1>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>15:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5></DRB5>
    <DQA1></DQA1>
    <DQB1>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:XX</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1></DPB1>
    </HLA>
    <IDM>
     <ANTI_CMV>P</ANTI_CMV>
     <ANTI_CMV_DATE>2010-07-04</ANTI_CMV_DATE>
     <CMV_NAT>N</CMV_NAT>
     <CMV_NAT_DATE>2010-07-04</CMV_NAT_DATE>
     <HBS_AG>N</HBS_AG>
     <ANTI_HBC>N</ANTI_HBC>
     <ANTI_HBS>N</ANTI_HBS>
     <ANTI_HCV>N</ANTI_HCV>
     <ANTI_HIV_12>N</ANTI_HIV_12>
     <HIV_1_NAT>N</HIV_1_NAT>
     <HIV_P24>N</HIV_P24>
     <HCV_NAT>N</HCV_NAT>
     <ANTI_HTLV>N</ANTI_HTLV>
     <SYPHILIS>N</SYPHILIS>
     <WNV>N</WNV>
     <CHAGAS>N</CHAGAS>
     <EBV>N</EBV>
     <TOXO>N</TOXO>
     <HBV_NAT>N</HBV_NAT>
     <PB19_NAT>N</PB19_NAT>
     <ALT>1</ALT>
    </IDM>
    <AL_SER>2</AL_SER>
    <SER_QUANT>10.0</SER_QUANT>
    <AL_PLA>3</AL_PLA>
    <PLA_QUANT>15.0</PLA_QUANT>
   </MAT>
  </CBU>
  </INVENTORY>
</INVENTORIES>

XSD 2.2 examples: (Expire in 2023, Q4)

Example donor file: ION-1234-D-XSD22.xml

Code Block

language	xml
title	Example Donor file XSD 2.2
linenumbers	true
collapse	true

<?xml version="1.0" encoding="UTF-8"?>
<INVENTORIES CREATION_TIME="2017-07-05T21:00:03Z">
 <INVENTORY LISTING_ORGANIZATION="1234" POOL="1234" CONTENT_TYPE="D" UPDATE_MODE="FULL" SNAPSHOT_TIME="2017-07-05T22:00:08Z" SCHEMA_VERSION="2.2">
  <DONOR>
   <ID>BMDW001</ID>
   <GRID>1234000000BMDW00101</GRID>
   <BIRTH_DATE>1962-02-10</BIRTH_DATE>
   <SEX>F</SEX>
   <ABO>O</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>CA</ETHN>
   <CCR5>DW</CCR5>
   <HLA>
    <A>
      <SER>
      <FIELD1>2</FIELD1>
      <FIELD2>11</FIELD2>
      </SER>
     <DNA>
      <FIELD1>02:CSAH</FIELD1>
      <FIELD2>11:MP</FIELD2>
     </DNA>
    </A>
    <B>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>39</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:XX</FIELD1>
      <FIELD2>39:KBY</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2></FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:HBA</FIELD1>
      <FIELD2>12:CF</FIELD2>
     </DNA>
    </C>
    <DRB1>
    <SER>
      <FIELD1>12</FIELD1>
      <FIELD2>15</FIELD2>
      </SER>
     <DNA>
      <FIELD1>12:GS</FIELD1>
      <FIELD2>15:CCZ</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5>
    <DNA>
    <FIELD1>01:01</FIELD1>
    <FIELD2></FIELD2>
    </DNA>
    </DRB5>
    <DQA1></DQA1>
    <DQB1>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>6</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:01</FIELD1>
      <FIELD2>06:02</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
     <DNA>
      <FIELD1>04:01</FIELD1>
      <FIELD2>03:01</FIELD2>
     </DNA>
    </DPB1>
   </HLA>
   <KIR>
    <KIR2DL1>NEG</KIR2DL1>
    <KIR2DL2>POS</KIR2DL2>
    <KIR2DL3>NEG</KIR2DL3>
    <KIR2DL4>NEG</KIR2DL4>
    <KIR2DL5A>NEG</KIR2DL5A>
    <KIR2DL5B>NEG</KIR2DL5B>
    <KIR2DS1>POS</KIR2DS1>
    <KIR2DS2>NEG</KIR2DS2>
    <KIR2DS3>NEG</KIR2DS3>
    <KIR2DS4>NEG</KIR2DS4>
    <KIR2DS5>NEG</KIR2DS5>
    <KIR2DP1>NEG</KIR2DP1>
    <KIR3DL1>NEG</KIR3DL1>
    <KIR3DL2>NEG</KIR3DL2>
    <KIR3DL3>NEG</KIR3DL3>
    <KIR3DS1>NEG</KIR3DS1>
    <KIR3DP1>NEG</KIR3DP1>
   </KIR>
   <IDM>
	<ANTI_CMV>H</ANTI_CMV>
	<ANTI_CMV_DATE>2016-06-24</ANTI_CMV_DATE>
	<CMV_NAT>P</CMV_NAT>
	<CMV_NAT_DATE>2016-06-24</CMV_NAT_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>1</ALT>
   </IDM>
   <STATUS>AV</STATUS>
   <CONTACT_DATE>2016-12-15</CONTACT_DATE>
   <WEIGHT>65</WEIGHT>
   <HEIGHT>175</HEIGHT>
   <NMBR_TRANS>1</NMBR_TRANS>
   <NMBR_PREG>1</NMBR_PREG>
   <NMBR_MARR>0</NMBR_MARR>
   <NMBR_PBSC>0</NMBR_PBSC>
   <COLL_TYPE>B</COLL_TYPE>
  </DONOR>
  <DONOR>
   <ID>BMDW002</ID>
   <GRID>1234000000BMDW00202</GRID>
   <BIRTH_DATE>1960-04-22</BIRTH_DATE>
   <SEX>M</SEX>
   <ABO>A</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>CA</ETHN>
   <CCR5>DD</CCR5>
   <HLA>
    <A>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>24</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:VJKM</FIELD1>
      <FIELD2>24:EJPF</FIELD2>
     </DNA>
    </A>
    <B>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>44</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:BCAU</FIELD1>
      <FIELD2>44:BCXE</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2></FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:ATGS</FIELD1>
      <FIELD2>16:01</FIELD2>
     </DNA>
    </C>
    <DRB1>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>15</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:DWH</FIELD1>
      <FIELD2>15:BMEG</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2></FIELD2>
     </DNA>
     </DRB5>
    <DQA1></DQA1>
    <DQB1>
    <SER>
      <FIELD1>2</FIELD1>
      <FIELD2>6</FIELD2>
      </SER>
     <DNA>
      <FIELD1>02:01</FIELD1>
      <FIELD2>06:02</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
     <DNA>
      <FIELD1>02:02</FIELD1>
      <FIELD2>03:01</FIELD2>
     </DNA>
    </DPB1>
   </HLA>
   <KIR>
   </KIR>
   <IDM>
	<ANTI_CMV>O</ANTI_CMV>
	<ANTI_CMV_DATE>2015-10-20</ANTI_CMV_DATE>
	<CMV_NAT>N</CMV_NAT>
	<CMV_NAT_DATE>2015-10-20</CMV_NAT_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>2</ALT>
   </IDM>
   <RSV_PAT>ABCD1234567</RSV_PAT>
   <STATUS>RS</STATUS>
   <STAT_END_DATE>2021-10-20</STAT_END_DATE>
   <STAT_REASON>TX</STAT_REASON>
   <CONTACT_DATE>2015-10-20</CONTACT_DATE>
   <CHECKUP_DATE>2015-10-20</CHECKUP_DATE>
   <WEIGHT>86</WEIGHT>
   <HEIGHT>187</HEIGHT>
   <NMBR_TRANS>0</NMBR_TRANS>
   <NMBR_MARR>0</NMBR_MARR>
   <NMBR_PBSC>1</NMBR_PBSC>
   <COLL_TYPE>B</COLL_TYPE>
  </DONOR>
 </INVENTORY>
</INVENTORIES>

Example CBU file: ION-1234-C-XSD22.xml

Code Block

language	xml
title	Example CBU file XSD 2.2
linenumbers	true
collapse	true

<?xml version="1.0" encoding="UTF-8"?>
<INVENTORIES CREATION_TIME="2017-07-05T21:00:04Z">
 <INVENTORY LISTING_ORGANIZATION="1234" POOL="1234" CONTENT_TYPE="C" UPDATE_MODE="FULL" SNAPSHOT_TIME="2017-07-05T22:00:05Z" SCHEMA_VERSION="2.2">
  <CBU>
   <ID>BMDW0CBU001</ID>
   <BIRTH_DATE>2009-09-02</BIRTH_DATE>
   <SEX>M</SEX>
   <ABO>A</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>AF</ETHN>
   <CCR5>DD</CCR5>
   <HLA>
    <A>
      <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>3</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:XX</FIELD1>
      <FIELD2>03:XX</FIELD2>
     </DNA>
    </A>
    <B>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>55</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:XX</FIELD1>
      <FIELD2>55:XX</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>7</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:03</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
    <DRB1>
    <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>15</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>15:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5>
    <DNA>
    <FIELD1>01:01</FIELD1>
    <FIELD2></FIELD2>
    </DNA>
    </DRB5>
    <DQA1></DQA1>
    <DQB1>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:02</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
    <DNA>
    <FIELD1>04:02</FIELD1>
    <FIELD2>11:01</FIELD2>
    </DNA>
    </DPB1>
   </HLA>
   <KIR>
    <KIR2DL1>NEG</KIR2DL1>
    <KIR2DL2>NEG</KIR2DL2>
    <KIR2DL3>NEG</KIR2DL3>
    <KIR2DL4>POS</KIR2DL4>
    <KIR2DL5A>NEG</KIR2DL5A>
    <KIR2DL5B>NEG</KIR2DL5B>
    <KIR2DS1>POS</KIR2DS1>
    <KIR2DS2>NEG</KIR2DS2>
    <KIR2DS3>NEG</KIR2DS3>
    <KIR2DS4>NEG</KIR2DS4>
    <KIR2DS5>NEG</KIR2DS5>
    <KIR2DP1>NEG</KIR2DP1>
    <KIR3DL1>NEG</KIR3DL1>
    <KIR3DL2>NEG</KIR3DL2>
    <KIR3DL3>NEG</KIR3DL3>
    <KIR3DS1>NEG</KIR3DS1>
    <KIR3DP1>NEG</KIR3DP1>
   </KIR>
   <IDM>
	<ANTI_CMV>N</ANTI_CMV>
    <ANTI_CMV_DATE>2009-09-04</ANTI_CMV_DATE>
    <CMV_NAT>N</CMV_NAT>
    <CMV_NAT_DATE>2009-09-04</CMV_NAT_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>1</ALT>
   </IDM>
   <STATUS>AV</STATUS>
   <LOCAL_ID>BMDW0CBU001</LOCAL_ID>
   <BAG_ID>BAG00BMDW001</BAG_ID>
   <BANK_MANUF_ID WMDA="6789" EMDIS="EN-38"></BANK_MANUF_ID>
   <BANK_DISTRIB_ID WMDA="6789" EMDIS="EN-38"></BANK_DISTRIB_ID>
   <COLL_DATE>2009-09-02</COLL_DATE>
   <PROC_DATE>2009-09-02</PROC_DATE>
   <PROC_METH>HES</PROC_METH>
   <PROC_METH_TYPE>SPX</PROC_METH_TYPE>
   <FREEZE_DATE>2009-09-02</FREEZE_DATE>
   <FREEZE_METH>C</FREEZE_METH>
   <PROD_MOD>PRR</PROD_MOD>
   <BAG_TYPE>80/20</BAG_TYPE>
   <BAGS>1</BAGS>
   <BACT_CULT>N</BACT_CULT>
   <FUNG_CULT>N</FUNG_CULT>
   <HEMO_STATUS>DN</HEMO_STATUS>
   <VOL>100</VOL>
   <VOL_FRZN>25</VOL_FRZN>
   <TNC>1.20E9</TNC>
   <TNC_FRZN>9.90E8</TNC_FRZN>
   <RED_BC_FRZN>9.00E7</RED_BC_FRZN>
   <MNC_FRZN>552999973</MNC_FRZN>
   <CD34PC>1.50E6</CD34PC>
   <CD34PC_FRZN>1.10E6</CD34PC_FRZN>
   <CFU_FRZN>1.23E6</CFU_FRZN>
   <VIABILITY>98</VIABILITY>
   <VIABILITY_DATE>2009-09-02</VIABILITY_DATE>
   <VIABILITY_CELLS>CD34PC</VIABILITY_CELLS>
   <VIABILITY_METHOD>7A</VIABILITY_METHOD>
   <ATT_SEG>2</ATT_SEG>
   <DNA_SMPL>true</DNA_SMPL>
   <OTH_SMPL>true</OTH_SMPL>
   <CT_COMPLETE_DATE>2016-09-22</CT_COMPLETE_DATE>
   <CT_SMPL_TYPE>ED</CT_SMPL_TYPE>
   <AL_RED_BC>3</AL_RED_BC>
   <AL_SER>4</AL_SER>
   <SER_QUANT>10.0</SER_QUANT>
   <AL_PLA>2</AL_PLA>
   <PLA_QUANT>10.0</PLA_QUANT>
   <MAT>
    <ID>123456789</ID>
    <ID_BANK>CBB01</ID_BANK>
    <HLA>
    <A>
      <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>68</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:XX</FIELD1>
      <FIELD2>68:XX</FIELD2>
     </DNA>
    </A>
    <B>
     <DNA>
      <FIELD1>07:XX</FIELD1>
      <FIELD2>39:XX</FIELD2>
     </DNA>
    </B>
    <C>
     <DNA>
      <FIELD1>12:03</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
    <DRB1>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>13:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5></DRB5>
    <DQA1></DQA1>
    <DQB1>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:03</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
    <DNA>
    <FIELD1>04:02</FIELD1>
    <FIELD2>11:01</FIELD2>
    </DNA>
    </DPB1>
    </HLA>
    <IDM>
     <ANTI_CMV>O</ANTI_CMV>
     <ANTI_CMV_DATE>2009-09-04</ANTI_CMV_DATE>
     <CMV_NAT>N</CMV_NAT>
     <CMV_NAT_DATE>2009-09-04</CMV_NAT_DATE>
     <HBS_AG>N</HBS_AG>
     <ANTI_HBC>N</ANTI_HBC>
     <ANTI_HBS>N</ANTI_HBS>
     <ANTI_HCV>N</ANTI_HCV>
     <ANTI_HIV_12>N</ANTI_HIV_12>
     <HIV_1_NAT>N</HIV_1_NAT>
     <HIV_P24>N</HIV_P24>
     <HCV_NAT>N</HCV_NAT>
     <ANTI_HTLV>N</ANTI_HTLV>
     <SYPHILIS>N</SYPHILIS>
     <WNV>N</WNV>
     <CHAGAS>N</CHAGAS>
     <EBV>G</EBV>
     <TOXO>N</TOXO>
     <HBV_NAT>N</HBV_NAT>
     <PB19_NAT>N</PB19_NAT>
     <ALT>2</ALT>
    </IDM>
    <AL_SER>2</AL_SER>
    <SER_QUANT>10.0</SER_QUANT>
    <AL_PLA>3</AL_PLA>
    <PLA_QUANT>15.0</PLA_QUANT>
   </MAT>
  </CBU>
  <CBU>
   <ID>BMDW0CBU002</ID>
   <BIRTH_DATE>2010-07-01</BIRTH_DATE>
   <SEX>F</SEX>
   <ABO>O</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>UK</ETHN>
   <CCR5>WW</CCR5>
   <HLA>
    <A>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>30</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:XX</FIELD1>
      <FIELD2>30:XX</FIELD2>
     </DNA>
    </A>
    <B>
      <SER>
      <FIELD1>8</FIELD1>
      <FIELD2>62</FIELD2>
      </SER>
     <DNA>
      <FIELD1>08:XX</FIELD1>
      <FIELD2>15:01</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>7</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:XX</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
    <DRB1>
    <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>13</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>13:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5></DRB5>
    <DQA1></DQA1>
    <DQB1>
    <SER>
      <FIELD1>5</FIELD1>
      <FIELD2>6</FIELD2>
      </SER>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:XX</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
    <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>04:01</FIELD2>
     </DNA></DPB1>
   </HLA>
   <KIR>
    <KIR2DL1>NEG</KIR2DL1>
    <KIR2DL2>POS</KIR2DL2>
    <KIR2DL3>NEG</KIR2DL3>
    <KIR2DL4>NEG</KIR2DL4>
    <KIR2DL5A>NEG</KIR2DL5A>
    <KIR2DL5B>NEG</KIR2DL5B>
    <KIR2DS1>POS</KIR2DS1>
    <KIR2DS2>NEG</KIR2DS2>
    <KIR2DS3>NEG</KIR2DS3>
    <KIR2DS4>NEG</KIR2DS4>
    <KIR2DS5>NEG</KIR2DS5>
    <KIR2DP1>NEG</KIR2DP1>
    <KIR3DL1>NEG</KIR3DL1>
    <KIR3DL2>NEG</KIR3DL2>
    <KIR3DL3>NEG</KIR3DL3>
    <KIR3DS1>NEG</KIR3DS1>
    <KIR3DP1>NEG</KIR3DP1>
   </KIR>
   <IDM>
    <ANTI_CMV>H</ANTI_CMV>
	<ANTI_CMV_DATE>2010-07-04</ANTI_CMV_DATE>
	<CMV_NAT>P</CMV_NAT>
	<CMV_NAT_DATE>2010-07-04</CMV_NAT_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>2</ALT>
   </IDM>
   <RSV_PAT>HHH0123</RSV_PAT>
   <STATUS>RS</STATUS>
   <STAT_END_DATE>2017-09-05</STAT_END_DATE>
   <STAT_REASON>OT</STAT_REASON>
   <LOCAL_ID>BMDW0CBU002</LOCAL_ID>
   <BAG_ID>BAG00MDW02</BAG_ID>
   <BANK_MANUF_ID WMDA="4567" EMDIS="EN-38"></BANK_MANUF_ID>
   <BANK_DISTRIB_ID WMDA="4567" EMDIS="EN-38"></BANK_DISTRIB_ID>
   <COLL_DATE>2010-07-01</COLL_DATE>
   <PROC_DATE>2010-07-01</PROC_DATE>
   <PROC_METH>HES</PROC_METH>
   <PROC_METH_TYPE>SPX</PROC_METH_TYPE>
   <FREEZE_DATE>2010-07-01</FREEZE_DATE>
   <FREEZE_METH>M</FREEZE_METH>
   <PROD_MOD>PLR</PROD_MOD>
   <BAG_TYPE>50/50</BAG_TYPE>
   <BAGS>1</BAGS>
   <BACT_CULT>N</BACT_CULT>
   <FUNG_CULT>N</FUNG_CULT>
   <HEMO_STATUS>DN</HEMO_STATUS>
   <VOL>49</VOL>
   <VOL_FRZN>25</VOL_FRZN>
   <TNC>5.71E8</TNC>
   <TNC_FRZN>4.33E8</TNC_FRZN>
   <RED_BC_FRZN>9.00E6</RED_BC_FRZN>
   <MNC_FRZN>340999990</MNC_FRZN>
   <CD34PC>2.0E6</CD34PC>
   <CD34PC_FRZN>1.70E6</CD34PC_FRZN>
   <CFU_FRZN>1.65E6</CFU_FRZN>
   <VIABILITY>97</VIABILITY>
   <VIABILITY_DATE>2010-07-02</VIABILITY_DATE>
   <VIABILITY_CELLS>CD34PC</VIABILITY_CELLS>
   <VIABILITY_METHOD>7A</VIABILITY_METHOD>
   <ATT_SEG>3</ATT_SEG>
   <DNA_SMPL>true</DNA_SMPL>
   <OTH_SMPL>true</OTH_SMPL>
   <CT_COMPLETE_DATE>2012-09-02</CT_COMPLETE_DATE>
   <CT_SMPL_TYPE>ED</CT_SMPL_TYPE>
   <AL_RED_BC>3</AL_RED_BC>
   <AL_SER>4</AL_SER>
   <SER_QUANT>10.0</SER_QUANT>
   <AL_PLA>2</AL_PLA>
   <PLA_QUANT>10.0</PLA_QUANT>
   <MAT>
    <ID>113456789-</ID>
    <ID_BANK>CBB001</ID_BANK>
    <HLA>
    <A>
     <DNA>
      <FIELD1>03:XX</FIELD1>
      <FIELD2>01:XX</FIELD2>
     </DNA>
    </A>
    <B>
      <SER>
      <FIELD1>8</FIELD1>
      <FIELD2>7</FIELD2>
      </SER>
     <DNA>
      <FIELD1>08:XX</FIELD1>
      <FIELD2>07:02</FIELD2>
     </DNA>
    </B>
    <C>
     <DNA>
      <FIELD1>07:02</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
    <DRB1>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>15:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5></DRB5>
    <DQA1></DQA1>
    <DQB1>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:XX</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1></DPB1>
    </HLA>
    <IDM>
     <ANTI_CMV>P</ANTI_CMV>
	 <ANTI_CMV_DATE>2010-07-04</ANTI_CMV_DATE>
	 <CMV_NAT>N</CMV_NAT>
	 <CMV_NAT_DATE>2010-07-04</CMV_NAT_DATE>
     <HBS_AG>N</HBS_AG>
     <ANTI_HBC>N</ANTI_HBC>
     <ANTI_HBS>N</ANTI_HBS>
     <ANTI_HCV>N</ANTI_HCV>
     <ANTI_HIV_12>N</ANTI_HIV_12>
     <HIV_1_NAT>N</HIV_1_NAT>
     <HIV_P24>N</HIV_P24>
     <HCV_NAT>N</HCV_NAT>
     <ANTI_HTLV>N</ANTI_HTLV>
     <SYPHILIS>N</SYPHILIS>
     <WNV>N</WNV>
     <CHAGAS>N</CHAGAS>
     <EBV>N</EBV>
     <TOXO>N</TOXO>
     <HBV_NAT>N</HBV_NAT>
     <PB19_NAT>N</PB19_NAT>
     <ALT>1</ALT>
    </IDM>
    <AL_SER>2</AL_SER>
    <SER_QUANT>10.0</SER_QUANT>
    <AL_PLA>3</AL_PLA>
    <PLA_QUANT>15.0</PLA_QUANT>
   </MAT>
  </CBU>
  </INVENTORY>
  </INVENTORIES>

XSD 2.1 examples: (Expired in 2021, Q4)

Code Block

language	xml
title	Example Donor file XSD 2.1 (Expire in Oct, 2021)
linenumbers	true
collapse	true

<?xml version="1.0" encoding="UTF-8"?>
<INVENTORIES CREATION_TIME="2017-07-05T21:00:03Z">
 <INVENTORY LISTING_ORGANIZATION="1234" POOL="1234" CONTENT_TYPE="D" UPDATE_MODE="FULL" SNAPSHOT_TIME="2017-07-05T22:00:08Z" SCHEMA_VERSION="2.1">
  <DONOR>
   <ID>BMDW001</ID>
   <GRID>1234000000BMDW00101</GRID>
   <BIRTH_DATE>1962-02-10</BIRTH_DATE>
   <SEX>F</SEX>
   <ABO>O</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>CA</ETHN>
   <CCR5>DW</CCR5>
   <HLA>
    <A>
      <SER>
      <FIELD1>2</FIELD1>
      <FIELD2>11</FIELD2>
      </SER>
     <DNA>
      <FIELD1>02:CSAH</FIELD1>
      <FIELD2>11:MP</FIELD2>
     </DNA>
    </A>
    <B>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>39</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:XX</FIELD1>
      <FIELD2>39:KBY</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2></FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:HBA</FIELD1>
      <FIELD2>12:CF</FIELD2>
     </DNA>
    </C>
    <DRB1>
    <SER>
      <FIELD1>12</FIELD1>
      <FIELD2>15</FIELD2>
      </SER>
     <DNA>
      <FIELD1>12:GS</FIELD1>
      <FIELD2>15:CCZ</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5>
    <DNA>
    <FIELD1>01:01</FIELD1>
    <FIELD2></FIELD2>
    </DNA>
    </DRB5>
    <DQA1></DQA1>
    <DQB1>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>6</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:01</FIELD1>
      <FIELD2>06:02</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
     <DNA>
      <FIELD1>04:01</FIELD1>
      <FIELD2>03:01</FIELD2>
     </DNA>
    </DPB1>
   </HLA>
   <KIR>
    <KIR2DL1>NEG</KIR2DL1>
    <KIR2DL2>POS</KIR2DL2>
    <KIR2DL3>NEG</KIR2DL3>
    <KIR2DL4>NEG</KIR2DL4>
    <KIR2DL5A>NEG</KIR2DL5A>
    <KIR2DL5B>NEG</KIR2DL5B>
    <KIR2DS1>POS</KIR2DS1>
    <KIR2DS2>NEG</KIR2DS2>
    <KIR2DS3>NEG</KIR2DS3>
    <KIR2DS4>NEG</KIR2DS4>
    <KIR2DS5>NEG</KIR2DS5>
    <KIR2DP1>NEG</KIR2DP1>
    <KIR3DL1>NEG</KIR3DL1>
    <KIR3DL2>NEG</KIR3DL2>
    <KIR3DL3>NEG</KIR3DL3>
    <KIR3DS1>NEG</KIR3DS1>
    <KIR3DP1>NEG</KIR3DP1>
   </KIR>
   <IDM>
    <CMV>H</CMV>
    <CMV_NAT>P</CMV_NAT>
    <CMV_DATE>2016-06-24</CMV_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>1</ALT>
   </IDM>
   <STATUS>AV</STATUS>
   <CONTACT_DATE>2016-12-15</CONTACT_DATE>
   <WEIGHT>65</WEIGHT>
   <HEIGHT>175</HEIGHT>
   <NMBR_TRANS>1</NMBR_TRANS>
   <NMBR_PREG>1</NMBR_PREG>
   <NMBR_MARR>0</NMBR_MARR>
   <NMBR_PBSC>0</NMBR_PBSC>
   <COLL_TYPE>B</COLL_TYPE>
  </DONOR>
  <DONOR>
   <ID>BMDW002</ID>
   <GRID>1234000000BMDW00202</GRID>
   <BIRTH_DATE>1960-04-22</BIRTH_DATE>
   <SEX>M</SEX>
   <ABO>A</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>CA</ETHN>
   <CCR5>DD</CCR5>
   <HLA>
    <A>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>24</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:VJKM</FIELD1>
      <FIELD2>24:EJPF</FIELD2>
     </DNA>
    </A>
    <B>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>44</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:BCAU</FIELD1>
      <FIELD2>44:BCXE</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2></FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:ATGS</FIELD1>
      <FIELD2>16:01</FIELD2>
     </DNA>
    </C>
    <DRB1>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>15</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:DWH</FIELD1>
      <FIELD2>15:BMEG</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2></FIELD2>
     </DNA>
     </DRB5>
    <DQA1></DQA1>
    <DQB1>
    <SER>
      <FIELD1>2</FIELD1>
      <FIELD2>6</FIELD2>
      </SER>
     <DNA>
      <FIELD1>02:01</FIELD1>
      <FIELD2>06:02</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
     <DNA>
      <FIELD1>02:02</FIELD1>
      <FIELD2>03:01</FIELD2>
     </DNA>
    </DPB1>
   </HLA>
   <KIR>
   </KIR>
   <IDM>
    <CMV>O</CMV>
    <CMV_NAT>N</CMV_NAT>
    <CMV_DATE>2015-10-20</CMV_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>2</ALT>
   </IDM>
   <RSV_PAT>ABCD1234567</RSV_PAT>
   <STATUS>RS</STATUS>
   <STAT_END_DATE>2017-10-20</STAT_END_DATE>
   <STAT_REASON>TX</STAT_REASON>
   <CONTACT_DATE>2015-10-20</CONTACT_DATE>
   <CHECKUP_DATE>2015-10-20</CHECKUP_DATE>
   <WEIGHT>86</WEIGHT>
   <HEIGHT>187</HEIGHT>
   <NMBR_TRANS>0</NMBR_TRANS>
   <NMBR_MARR>0</NMBR_MARR>
   <NMBR_PBSC>1</NMBR_PBSC>
   <COLL_TYPE>B</COLL_TYPE>
  </DONOR>
 </INVENTORY>
</INVENTORIES>

Code Block

language	xml
title	Example CBU file XSD 2.1 (Expire Oct, 2021)
linenumbers	true
collapse	true

<?xml version="1.0" encoding="UTF-8"?>
<INVENTORIES CREATION_TIME="2017-07-05T21:00:04Z">
 <INVENTORY LISTING_ORGANIZATION="1234" POOL="1234" CONTENT_TYPE="C" UPDATE_MODE="FULL" SNAPSHOT_TIME="2017-07-05T22:00:05Z" SCHEMA_VERSION="2.1">
  <CBU>
   <ID>BMDW0CBU001</ID>
   <BIRTH_DATE>2009-09-02</BIRTH_DATE>
   <SEX>M</SEX>
   <ABO>A</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>AF</ETHN>
   <CCR5>DD</CCR5>
   <HLA>
    <A>
      <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>3</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:XX</FIELD1>
      <FIELD2>03:XX</FIELD2>
     </DNA>
    </A>
    <B>
    <SER>
      <FIELD1>7</FIELD1>
      <FIELD2>55</FIELD2>
      </SER>
     <DNA>
      <FIELD1>07:XX</FIELD1>
      <FIELD2>55:XX</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>7</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:03</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
    <DRB1>
    <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>15</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>15:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5>
    <DNA>
    <FIELD1>01:01</FIELD1>
    <FIELD2></FIELD2>
    </DNA>
    </DRB5>
    <DQA1></DQA1>
    <DQB1>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:02</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
    <DNA>
    <FIELD1>04:02</FIELD1>
    <FIELD2>11:01</FIELD2>
    </DNA>
    </DPB1>
   </HLA>
   <KIR>
    <KIR2DL1>NEG</KIR2DL1>
    <KIR2DL2>NEG</KIR2DL2>
    <KIR2DL3>NEG</KIR2DL3>
    <KIR2DL4>POS</KIR2DL4>
    <KIR2DL5A>NEG</KIR2DL5A>
    <KIR2DL5B>NEG</KIR2DL5B>
    <KIR2DS1>POS</KIR2DS1>
    <KIR2DS2>NEG</KIR2DS2>
    <KIR2DS3>NEG</KIR2DS3>
    <KIR2DS4>NEG</KIR2DS4>
    <KIR2DS5>NEG</KIR2DS5>
    <KIR2DP1>NEG</KIR2DP1>
    <KIR3DL1>NEG</KIR3DL1>
    <KIR3DL2>NEG</KIR3DL2>
    <KIR3DL3>NEG</KIR3DL3>
    <KIR3DS1>NEG</KIR3DS1>
    <KIR3DP1>NEG</KIR3DP1>
   </KIR>
   <IDM>
   <CMV>N</CMV>
    <CMV_NAT>N</CMV_NAT>
    <CMV_DATE>2009-09-04</CMV_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>1</ALT>
   </IDM>
   <STATUS>AV</STATUS>
   <LOCAL_ID>BMDW0CBU001</LOCAL_ID>
   <BAG_ID>BAG00BMDW001</BAG_ID>
   <BANK_MANUF_ID>6789</BANK_MANUF_ID>
   <BANK_DISTRIB_ID>6789</BANK_DISTRIB_ID>
   <COLL_DATE>2009-09-02</COLL_DATE>
   <PROC_DATE>2009-09-02</PROC_DATE>
   <PROC_METH>HES</PROC_METH>
   <PROC_METH_TYPE>SPX</PROC_METH_TYPE>
   <FREEZE_DATE>2009-09-02</FREEZE_DATE>
   <FREEZE_METH>C</FREEZE_METH>
   <PROD_MOD>PRR</PROD_MOD>
   <BAG_TYPE>80/20</BAG_TYPE>
   <BAGS>1</BAGS>
   <BACT_CULT>N</BACT_CULT>
   <FUNG_CULT>N</FUNG_CULT>
   <HEMO_STATUS>DN</HEMO_STATUS>
   <VOL>100</VOL>
   <VOL_FRZN>25</VOL_FRZN>
   <TNC>1.20E9</TNC>
   <TNC_FRZN>9.90E8</TNC_FRZN>
   <RED_BC_FRZN>9.00E7</RED_BC_FRZN>
   <MNC_FRZN>552999973</MNC_FRZN>
   <CD34PC>1.50E6</CD34PC>
   <CD34PC_FRZN>1.10E6</CD34PC_FRZN>
   <CFU_FRZN>1.23E6</CFU_FRZN>
   <VIABILITY>98</VIABILITY>
   <VIABILITY_DATE>2009-09-02</VIABILITY_DATE>
   <VIABILITY_CELLS>CD34PC</VIABILITY_CELLS>
   <VIABILITY_METHOD>7A</VIABILITY_METHOD>
   <ATT_SEG>2</ATT_SEG>
   <DNA_SMPL>true</DNA_SMPL>
   <OTH_SMPL>true</OTH_SMPL>
   <CT_COMPLETE_DATE>2016-09-22</CT_COMPLETE_DATE>
   <CT_SMPL_TYPE>ED</CT_SMPL_TYPE>
   <AL_RED_BC>3</AL_RED_BC>
   <AL_SER>4</AL_SER>
   <SER_QUANT>10.0</SER_QUANT>
   <AL_PLA>2</AL_PLA>
   <PLA_QUANT>10.0</PLA_QUANT>
   <MAT>
    <ID>123456789</ID>
    <ID_BANK>CBB01</ID_BANK>
    <HLA>
    <A>
      <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>68</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:XX</FIELD1>
      <FIELD2>68:XX</FIELD2>
     </DNA>
    </A>
    <B>
     <DNA>
      <FIELD1>07:XX</FIELD1>
      <FIELD2>39:XX</FIELD2>
     </DNA>
    </B>
    <C>
     <DNA>
      <FIELD1>12:03</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
    <DRB1>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>13:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5></DRB5>
    <DQA1></DQA1>
    <DQB1>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:03</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
    <DNA>
    <FIELD1>04:02</FIELD1>
    <FIELD2>11:01</FIELD2>
    </DNA>
    </DPB1>
    </HLA>
    <IDM>
     <CMV>O</CMV>
     <CMV_NAT>N</CMV_NAT>
     <CMV_DATE>2009-09-04</CMV_DATE>
     <HBS_AG>N</HBS_AG>
     <ANTI_HBC>N</ANTI_HBC>
     <ANTI_HBS>N</ANTI_HBS>
     <ANTI_HCV>N</ANTI_HCV>
     <ANTI_HIV_12>N</ANTI_HIV_12>
     <HIV_1_NAT>N</HIV_1_NAT>
     <HIV_P24>N</HIV_P24>
     <HCV_NAT>N</HCV_NAT>
     <ANTI_HTLV>N</ANTI_HTLV>
     <SYPHILIS>N</SYPHILIS>
     <WNV>N</WNV>
     <CHAGAS>N</CHAGAS>
     <EBV>G</EBV>
     <TOXO>N</TOXO>
     <HBV_NAT>N</HBV_NAT>
     <PB19_NAT>N</PB19_NAT>
     <ALT>2</ALT>
    </IDM>
    <AL_SER>2</AL_SER>
    <SER_QUANT>10.0</SER_QUANT>
    <AL_PLA>3</AL_PLA>
    <PLA_QUANT>15.0</PLA_QUANT>
   </MAT>
  </CBU>
  <CBU>
   <ID>BMDW0CBU002</ID>
   <BIRTH_DATE>2010-07-01</BIRTH_DATE>
   <SEX>F</SEX>
   <ABO>O</ABO>
   <RHESUS>P</RHESUS>
   <ETHN>UK</ETHN>
   <CCR5>WW</CCR5>
   <HLA>
    <A>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>30</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:XX</FIELD1>
      <FIELD2>30:XX</FIELD2>
     </DNA>
    </A>
    <B>
      <SER>
      <FIELD1>8</FIELD1>
      <FIELD2>62</FIELD2>
      </SER>
     <DNA>
      <FIELD1>08:XX</FIELD1>
      <FIELD2>15:01</FIELD2>
     </DNA>
    </B>
    <C>
    <SER>
      <FIELD1>3</FIELD1>
      <FIELD2>7</FIELD2>
      </SER>
     <DNA>
      <FIELD1>03:XX</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
    <DRB1>
    <SER>
      <FIELD1>1</FIELD1>
      <FIELD2>13</FIELD2>
      </SER>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>13:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5></DRB5>
    <DQA1></DQA1>
    <DQB1>
    <SER>
      <FIELD1>5</FIELD1>
      <FIELD2>6</FIELD2>
      </SER>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:XX</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1>
    <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>04:01</FIELD2>
     </DNA></DPB1>
   </HLA>
   <KIR>
    <KIR2DL1>NEG</KIR2DL1>
    <KIR2DL2>POS</KIR2DL2>
    <KIR2DL3>NEG</KIR2DL3>
    <KIR2DL4>NEG</KIR2DL4>
    <KIR2DL5A>NEG</KIR2DL5A>
    <KIR2DL5B>NEG</KIR2DL5B>
    <KIR2DS1>POS</KIR2DS1>
    <KIR2DS2>NEG</KIR2DS2>
    <KIR2DS3>NEG</KIR2DS3>
    <KIR2DS4>NEG</KIR2DS4>
    <KIR2DS5>NEG</KIR2DS5>
    <KIR2DP1>NEG</KIR2DP1>
    <KIR3DL1>NEG</KIR3DL1>
    <KIR3DL2>NEG</KIR3DL2>
    <KIR3DL3>NEG</KIR3DL3>
    <KIR3DS1>NEG</KIR3DS1>
    <KIR3DP1>NEG</KIR3DP1>
   </KIR>
   <IDM>
   <CMV>N</CMV>
    <CMV_NAT>N</CMV_NAT>
    <CMV_DATE>2010-07-04</CMV_DATE>
    <HBS_AG>N</HBS_AG>
    <ANTI_HBC>N</ANTI_HBC>
    <ANTI_HBS>N</ANTI_HBS>
    <ANTI_HCV>N</ANTI_HCV>
    <ANTI_HIV_12>N</ANTI_HIV_12>
    <HIV_1_NAT>N</HIV_1_NAT>
    <HIV_P24>N</HIV_P24>
    <HCV_NAT>N</HCV_NAT>
    <ANTI_HTLV>N</ANTI_HTLV>
    <SYPHILIS>N</SYPHILIS>
    <WNV>N</WNV>
    <CHAGAS>N</CHAGAS>
    <EBV>H</EBV>
    <TOXO>N</TOXO>
    <HBV_NAT>N</HBV_NAT>
    <PB19_NAT>N</PB19_NAT>
    <ALT>2</ALT>
   </IDM>
   <RSV_PAT>HHH0123</RSV_PAT>
   <STATUS>RS</STATUS>
   <STAT_END_DATE>2017-09-05</STAT_END_DATE>
   <STAT_REASON>OT</STAT_REASON>
   <LOCAL_ID>BMDW0CBU002</LOCAL_ID>
   <BAG_ID>BAG00MDW02</BAG_ID>
   <BANK_MANUF_ID>4567</BANK_MANUF_ID>
   <BANK_DISTRIB_ID>4567</BANK_DISTRIB_ID>
   <COLL_DATE>2010-07-01</COLL_DATE>
   <PROC_DATE>2010-07-01</PROC_DATE>
   <PROC_METH>HES</PROC_METH>
   <PROC_METH_TYPE>SPX</PROC_METH_TYPE>
   <FREEZE_DATE>2010-07-01</FREEZE_DATE>
   <FREEZE_METH>M</FREEZE_METH>
   <PROD_MOD>PLR</PROD_MOD>
   <BAG_TYPE>50/50</BAG_TYPE>
   <BAGS>1</BAGS>
   <BACT_CULT>N</BACT_CULT>
   <FUNG_CULT>N</FUNG_CULT>
   <HEMO_STATUS>DN</HEMO_STATUS>
   <VOL>49</VOL>
   <VOL_FRZN>25</VOL_FRZN>
   <TNC>5.71E8</TNC>
   <TNC_FRZN>4.33E8</TNC_FRZN>
   <RED_BC_FRZN>9.00E6</RED_BC_FRZN>
   <MNC_FRZN>340999990</MNC_FRZN>
   <CD34PC>2.0E6</CD34PC>
   <CD34PC_FRZN>1.70E6</CD34PC_FRZN>
   <CFU_FRZN>1.65E6</CFU_FRZN>
   <VIABILITY>97</VIABILITY>
   <VIABILITY_DATE>2010-07-02</VIABILITY_DATE>
   <VIABILITY_CELLS>CD34PC</VIABILITY_CELLS>
   <VIABILITY_METHOD>7A</VIABILITY_METHOD>
   <ATT_SEG>3</ATT_SEG>
   <DNA_SMPL>true</DNA_SMPL>
   <OTH_SMPL>true</OTH_SMPL>
   <CT_COMPLETE_DATE>2012-09-02</CT_COMPLETE_DATE>
   <CT_SMPL_TYPE>ED</CT_SMPL_TYPE>
   <AL_RED_BC>3</AL_RED_BC>
   <AL_SER>4</AL_SER>
   <SER_QUANT>10.0</SER_QUANT>
   <AL_PLA>2</AL_PLA>
   <PLA_QUANT>10.0</PLA_QUANT>
   <MAT>
    <ID>113456789-</ID>
    <ID_BANK>CBB001</ID_BANK>
    <HLA>
    <A>
     <DNA>
      <FIELD1>03:XX</FIELD1>
      <FIELD2>01:XX</FIELD2>
     </DNA>
    </A>
    <B>
      <SER>
      <FIELD1>8</FIELD1>
      <FIELD2>7</FIELD2>
      </SER>
     <DNA>
      <FIELD1>08:XX</FIELD1>
      <FIELD2>07:02</FIELD2>
     </DNA>
    </B>
    <C>
     <DNA>
      <FIELD1>07:02</FIELD1>
      <FIELD2>07:XX</FIELD2>
     </DNA>
    </C>
    <DRB1>
     <DNA>
      <FIELD1>01:01</FIELD1>
      <FIELD2>15:XX</FIELD2>
     </DNA>
    </DRB1>
    <DRB3></DRB3>
    <DRB4></DRB4>
    <DRB5></DRB5>
    <DQA1></DQA1>
    <DQB1>
     <DNA>
      <FIELD1>05:01</FIELD1>
      <FIELD2>06:XX</FIELD2>
     </DNA>
    </DQB1>
    <DPA1></DPA1>
    <DPB1></DPB1>
    </HLA>
    <IDM>
     <CMV>P</CMV>
     <CMV_NAT>N</CMV_NAT>
     <CMV_DATE>2010-07-04</CMV_DATE>
     <HBS_AG>N</HBS_AG>
     <ANTI_HBC>N</ANTI_HBC>
     <ANTI_HBS>N</ANTI_HBS>
     <ANTI_HCV>N</ANTI_HCV>
     <ANTI_HIV_12>N</ANTI_HIV_12>
     <HIV_1_NAT>N</HIV_1_NAT>
     <HIV_P24>N</HIV_P24>
     <HCV_NAT>N</HCV_NAT>
     <ANTI_HTLV>N</ANTI_HTLV>
     <SYPHILIS>N</SYPHILIS>
     <WNV>N</WNV>
     <CHAGAS>N</CHAGAS>
     <EBV>N</EBV>
     <TOXO>N</TOXO>
     <HBV_NAT>N</HBV_NAT>
     <PB19_NAT>N</PB19_NAT>
     <ALT>1</ALT>
    </IDM>
    <AL_SER>2</AL_SER>
    <SER_QUANT>10.0</SER_QUANT>
    <AL_PLA>3</AL_PLA>
    <PLA_QUANT>15.0</PLA_QUANT>
   </MAT>
  </CBU>
  </INVENTORY>
  </INVENTORIES>

Validation of your XML files

After generating your XML files, you are advised to validate the generated XML file. You may use any XML tool that includes validation for that, for example the open source Qxmledit or XMLLINT.

You can use xmllint by invoking the program giving the XML file and the Schema file, and it will generate a report.

If the file validates, it will show:

Code Block
xmllint --schema Inventories.xsd --huge --stream --sax --noout ION-1234-C.xml ION-1234-C.xml validates

If it does not validate, you will see what XSD rule is violated, together with the line where that happened eg:

Code Block
410460: Schemas validity error : Element 'CCR5': [facet 'enumeration'] The value '' is not an element of the set {'DD', 'WW', 'DW'}.

Expand

title	Read more on installing XMLLINT on Windows

Installing XMLLINT on Windows is a bit tricky, you will need the XSD files, and a set of binaries from http://xmlsoft.org/sources/win32/ for 32bit system, or http://xmlsoft.org/sources/win32/64bit for 64bit system.

Download the XSD files.
Download the required binary files.
You need the binary files from 4 .zip files, and download the latest version. They are iconv, libxml2, libxslt and zlib.
The names are as belows, some binary files may have suffix version number, that is fine, and you can keep it.
Code Block
basicTypes.xsd Inventories.xsd iconv.exe libcharset-1.dll libiconv-2.dll libxml2-2.dll xml2-config xmlcatalog.exe xmllint.exe zlib1.dll
Create a new folder in C:\tools\libxml. (This is a suggestion from the owner). Or you can create folder "libxml" in C:\Windows\ or C:\Program Files as you prefer.
Move all binary files in the folder C:\tools\libxml
Add "C:\tools\libxml" to the System environment variable PATH/Path.
Restart your system
The xmllint cmds can be executed in the windows cmd or PowerShell (windows 10).

Please refer to your IT staff for installation if you can not handle this.

Viewing large files

XML files tend to be large. For quick visual inspection and search you may use Glogg (windows)

Generate XML file from excel data source

WMDA suggest two methods to generate the XML file manually for small dataset.

If you have Microsoft excel with developer tab. You can manually generate the XML with less than 65,536 records. You can use the specific xsd schema file Inventories-cbu-xml-gen.xsd or Inventories-donor-xml-gen.xsd to generate the XML file.
You can download the file mentioned above in the XSD schema page.
WMDA prepare a php script to generate XML file from excel/csv data source for small dataset like less than 2000 records. If you need further help, please contact support@wmda.info.

Tab Pane | Vectors (Formerly: SP Tab pane)

anchor	1965969468
name	File names

#

File names

Registries with data on stem cell donors and cord blood units should separate these two data sets and provide two files: one for stem cell donors, and one for cord blood units. Data of stem cell donors and cord blood units should not be combined in one file. In the filename the distinction between donor data and cord blood unit data is made clear.

The first part of the filename is "ION-" (without the quotes) followed by the ion number and either a "D-" for donors (without the quotes) or a "C-" (without the quotes) for cold blood units. This <ION> should be similar to the one provided in the field <POOL>. The extension of the file is ".XML". Using this naming convention the name of the Austrian cord blood registry is: ION-2614-C.XML and the name of the German donor registry is: ION-6939-D.XML

After encryption, the file should follow almost the same name convention as for the xml file name, but then xml is replaced to pgp. So the first part of the GPG-filename is identical to the XML-filename. The GPG software will either add a second extension ".PGP", or replace the ".XML" extension of the data file with the ".PGP" extension. As an example, the file name of an encrypted Austrian cord blood file would then be: "ION-2614-C.PGP" (without the quotes).

If you are listing organisation and are also sending data from other listing organisations (with ION), you can provide the inventory of different POOL IDs together in one file. However, you should not combine donor and CBU data together. For the file naming, please always use the ION from the organisation that is sending the data.

Tab Pane | Vectors (Formerly: SP Tab pane)

anchor	124682242
name	ZIP (compress) file

#

How to compress your XML file with ZIP

Info
ZIP file is not a request anymore, even for big file. Because the encryption process will compress and encrypt the file.

When your file is larger then 200Mb, you have to compress your file by using ZIP. If your file is smaller, you are also encouraged to compress your file, because the time to upload your file will be reduced.

Please find below some methods to compress your file with ZIP when you are using any of the operating systems Windows, OS, or Linux/unix.

Please note: When you are using another method to compress your file, like tar, we cannot decompress your file during processing and we have to reject the file.

Creating a compressed zip file in Windows

Click to highlight the file that you need to zip. Please note: WMDA can only accept your file when the zip file contains 1 file.
Right-click the file and select Send to > Compressed (zipped) Folder.
Windows will create the zip file and will position the cursor where you can choose a unique name for the file.

It is also possible to first create your ZIP folder and then drag the file to your zip folder.

Creating a compressed zip file in OS X

Open a new Finder window and navigate to the file.
Click to highlight the file that you need to zip.
Select File > Compress from the pull-down menu. Sometimes you can also click with your right mouse button on the file and use the quick menu.
Finder will compress the selected file and will create the zip file with the same same as your file but with the extension .zip.

Creating a compressed zip file in Linux

Open a terminal session and navigate to the location of your file
To view a listing of directory contents, enter the following command: ls
Note the files to be zipped.
Create the zip file by entering the command: zip {.zip-filename} {filename-to-compress} (e.g. zip ION-1234-D.zip ION-1234-D.xml)

Tab Pane | Vectors (Formerly: SP Tab pane)

anchor	1844199817
name	Encrypt file

#

How to encrypt your XML file

WMDA will only accept pgp encrypted XML files for data upload. We will now describe how you can encrypt your xml file. If you have a very large file, you should first compress your file with ZIP before you encrypt your file. Please see the picture below for a schematic representation of the encryption en decryption process.

Encryption is performed by the organisation who is sending data to WMDA; decryption is performed by WMDA to be able to process and validate the data in your file.

For this encryption, you should use the WMDA public key.

This is the new public key: public key (download the file in this link)

You may also fetch the key from the link or the https://keys.openpgp.org/vks/v1/by-fingerprint/B83744C5CE38C10265E36120C44E0E7A736E374E
(Notice can not be searched by dataupload@wmda.info, as it dose not exist, and not verified)

Expand

title	See more key details ..

Public key details : Key ID C44E0E7A736E374E

Fingerprint = B837 44C5 CE38 C102 65E3 6120 C44E 0E7A 736E 374

userid = "dataupload.wmda.info <dataupload@wmda.info>"

Code Block

title	PGP Public key for XML

Please note: This key is different from the key that you used to encrypt your DOT20 file.

STEP 1: Encryption program

The DOT20 file also needed to be encrypted. The procedure is actually the same, but you now have to use the new public key.

Currently, there are several different software packages that you can use to encrypt and decrypt your files. It depends of course also of your operating system which programs you can use.

Here are some examples:

Windows: Kleopatra (download here), PGP Tool

OS (MAC): GPG Suite

Linux/unix: GnuPG

GnuPG is a complete and free implementation of the OpenPGP standard as defined by RFC4880 (also known as PGP ). GnuPG allows to encrypt and sign your data and communication, features a versatile key management system as well as access modules for all kinds of public key directories. GnuPG, also known as GPG , is a command line tool with features for easy integration with other applications. A wealth of frontend applications and libraries are available. GnuPG is Free Software (meaning that it respects your freedom). It can be freely used, modified and distributed under the terms of the GNU General Public License . For installation on your Linux/Unix machine, please visit the following page for HowTos: https://www.gnupg.org/documentation/howtos.html

STEP 2: Import the public key

After installing your preferred program, you have to import the public key.

First download the public key to your computer. It is important that you save the file with extension asc (key.asc)
Open your encryption program and look for something like import (PGP) key or import certificate. Click on this and then you have to upload the file with the WMDA public key and save the key.
If you might get an error with importing the key, you can try to remove the text “Version: GnuPG v2” from the file and try to import the file again.

For Linux/Unix, importing of the key in your gpg keyring can be done by using the following command:

$ gpg --import {public_key_file}

Alternatively, instead of saving this file and importing the key, you may look it up at a keyserver.

For example, if you use Kleopatra, use CTRL-SHIFT-I and search for 0xC44E0E7A736E374E

Getting the key :http https://poolkeyserver.sks-keyserversubuntu.netcom/pks/lookup?search=0xC44E0E7A736E374E&fingerprint=on&op=index

If you use gpg from the commandline, use gpg --recv-keys --keyserver keyserverpool.sks-keyservers.netubuntu.com --recv 0xC44E0E7A736E374E

STEP 3: Encrypt XML or ZIP file with the public key

Next step is to use the public key that you just imported into your encryption program to encrypt your XML or zipped XML file.

In your encryption program, go to the function called encrypt or encrypt files.
A windows with all your files will open. Look up the file you would like to encrypt.
Following the steps in your program and make sure you choose the public key to encrypt your file

Some programs work together with your file exploring program like Finder for Mac or Explorer for windows. If this is the case, go to your file look-up program and look for your file.
Select your file and click on the right mouse button. A quick menu will become visible. Look for something with encryption or GPG or with a MAC it is probably under Services. This depends on the program you installed on your computer. Click on that and follow the instructions on your screen.
Make sure you choose the public key to encrypt your file.

For Linux/Unix, encryption of your file can be done by using the following command:

$ gpg --encrypt --recipient ID {filename_to_be_encrypted}

where ID is replaced with that key's ID

The short version of the above command is:

$ gpg -e -r ID {filename_to_be_encrypted}

In either case, a file is created with the same name, plus an additional .gpg file extension added to the end. Thus, if your file is ION-1234-D.xml, you will create an encrypted copy of the file named ION-1234-D.xml.gpg.

Please note: Do not sign your file. This will result in rejection of your file during processing.

User guide for Kleopatra(Windows):

Download here. It is included in the gpg4win package.
Import the the public key. And you will see imported public key as below:
Encrypt the file. Click "Sign/Encrypt", in the pop-up window, un-check "Sign as", "Encrypt for me" and "Encrypt with password".

And in "Encrypt for others", type in the public key e-mails to get the public key.
Tip: if the WMDA public key is imported correctly, then after you type-in "data", the whole key name will pop-up, and can be selected.
NOTE: There will be pop-up window to notify you to certify the public key, you can ignore this. But if you do want to certify the public key, you can following the guide here.
If the public key is correctly imported, but without certify, there will be a blue "i" icon () in front of the key. If you add certify, then it will be green "v" icon.
If the public key is not correctly imported, there will be a red "x" icon(). If that is the case, please repeat above process till you see the .

After that, the grep "next" button will turn "Encrypt", then click "Encrypt" to encrypt the file. You may get warning that you can not decrypt the file because you do not have private key, that is fine.

Tab Pane | Vectors (Formerly: SP Tab pane)

anchor	555255290
name	Data Validation: Errors and warnings in processing report

#

Explanation of Errors and Warnings in your processing report

Info

title	INFORMATION

We are currently working on the new errors and warning you might find in your processing report. The errors and warnings shown below are mainly based on the old processing reports and are amended to our best knowledge at this moment. More information will follow soon.

After submitting a file you will receive a processing report in your data upload service account. This document describes explanations of warnings or errors as you may find them in the processing report. In the explanations below you find references to various fields from the file format for data delivery. For details on these field names and the file format look in the tabs 'XML file' and 'File name' of this page.

The ID of the donor or CBU will be displayed as well. This helps you find the problem line in the file you have sent, and hopefully helps you correct the problem.

Business validation rules applied

WMDA has additional business validation rules in place to ensure that even though the data supplied on a field level might be correct they need to have passed the validation rules applied sometimes on multiple fields to ensure correct data is being added to the GCD database. As part of providing us the XML your organisation should also perform these checks to ensure the validity of the data you are providing.

Business validation rules in excel file

ConfiForms TableView

filter	ValidationSource.label:BMDW
withHighlighting	true
enableFilterSupport	true
pageTitle	Business rules Input form XML files-(member Public)
formName	ValidationRulesXMLMemberAccess
sort	ValidationLevel ASC, ValidationSource ASC
wrapped	true
export	true
enableSearch	true

Een dropdown heeft altijd een
value en een label :
Bij het opzetten van het veld heb je gekozen voor numerieke value, en tekstuele labels, dwz

als je "BMDW" ziet, staat er in de form "1"

Bij het filteren van de table moet je dus ofwel

filter = ValidationSource.label:BMDW

of

filter = ValidationSource:1
kiezen.

Reference numberRefNumber

Validation levelValidationLevel

Validation sourceValidationSource

Date rule is validDateValid

Effective since XSD version numberXSDEffectiveVersionNo

Field nameFieldName

Error in fieldErrorInField

Reported validation messageReportedValidationMessage

Action

File Errors

FileError: Empty file or file without data.

Explanation: When the size of the received file is zero bytes, or no data could be read from the received file, this error is returned.

Record Errors

RecordError: No ID specified: Explanation: The ID or GRID field should be given, and should not be blank.
RecordError: Duplicate donor/CBU ID found: Explanation: Every donor or cord blood unit should be listed only once. During processing of your file, a donor or cord blood ID is listed more than once, only the first occurrence has been accepted. The second occurrence XXXXX has been rejected.
RecordError: Invalid GRID ID specified: Explanation: The global registration identified provided is invalid. PLEASE NOTE: GRID format allowed is: XXXX XXXX XXXX XXXX XXX. Also only upper case letter and numbers are allowed.
RecordError: Duplicate GRID ID found: Explanation: Every donor or cord blood unit should be listed only once. During processing of your file, a GRID ID is listed more than once, only the first occurrence has been accepted. The second occurrence XXXXX has been rejected.
RecordError: Invalid ION & GRID specified: Explanation: The GRID ID and Listing organisation (ION) ID are contradictory.
RecordError: "Collected Volume before processing" (VOL) has an incorrect value: Explanation: The "Volume Collected" (VOL) should be no less than 10, or more than 400 milliliters (ml).
RecordError: "Total Nucleated Cells" (TNC) has an incorrect value: Explanation: The "Total Nucleated Cells" should be no less than 10, or more than 999 (10^7).
RecordError: "Collected number of CD34+ cells" (CD34PC) has an incorrect value: Explanation: The value provided for the CD34+ cell count is not a numeric value with decimal point in units of 10^6.
RecordError: "Collected number of mononuclear cells" (MNC_FRZN) has an incorrect value: Explanation: The value provided for the mononucleated cell count is rounded number of mononuclear cells in the units of 10^7.
RecordError: Duplicate donor/CBU ID found: Explanation: Every donor or cord blood unit should be listed only once. If during processing of a file, a donor or cord blood ID is listed more than once, only the first occurrence is accepted, the second occurrence generates this error.
RecordError: Invalid date format for field 'field name' given: Explanation:This error may be returned for date fields. The format for dates field should be in the format YYYY-MM-DD.
RecordError: Donor is either too young or too old: Explanation:The age limits of donors are set by the WMDA. Donor age outside range of 18-60 years are rejected.
RecordError: Invalid Gender value found (not "M" or "F"): Explanation: Gender of donors other than "M" (for Male) or "F" (for Female) are reported as an error.
RecordError: Invalid CMV Status value found: Explanation: The CMV status provided is not one of the possible values for this field.
RecordError: BANK_MANUF_ID not provided: Explanation: The BANK_MANUF_ID allows the Search report to indicate that the Cord blood bank unit is accredited. If you do not provide this ID the search report will not be able to indicate the cord blood bank unit as being accredited or not.

HLA/DNA Related Errors

HLA/DNA-ERROR: Invalid allele value X found for DNA-"Allele".

Example: <HLA><DRB4><DNA><FIELD1>01:01/</FIELD1><FIELD2>value</FIELD2></DNA></DRB4></HLA>

Explanation: The value for DRB4 contains a slash (/) which is invalid. If such a problem is found the allele values are blanked and processing of the record continues. So, this is a warning, and not an error that requires the record to be rejected!Another examples might be an C*04:AVK (AVK is assigned bij the NMDP as 01/02/03/04/05/06) which is not valid since the C*04:02 is not assigned.

HLA/DNA-ERROR: Invalid DNA string found: "some string"

Example: For HLA A, the following value is given: 01:01/01:02/01:03/01:04.

Explanation: The DNA string given A*01:01/01:02/01:03/01:04 is not valid since the A*01:04 does not exist. Another reported problem may be that a ambiguity in the format of A*01:01/02/03 is invalid.

HLA/DNA-ERROR: Invalid HLA antigen "some value" found for field "field name".

Example: Serological HLA A30/3 is given in the file.

Explanation: The antigen or search determinant value "30/3" for HLA-A in this example is invalid.

HLA/DNA-ERROR: Incomplete typing found: HLA-A and HLA-B are required.

Explanation: At least one HLA-A and -B antigen or serological value should be available to be able to match the record. If no HLA-A or -B values (either on DNA level or on serological level) are available the record is rejected.

HLA/DNA-ERROR: "DNA allele values" does not match "serology". Equivalents for DNA alleles are ...

Example: HLA-B*15:02,15:26N does not match serological HLA-B76,62. Equivalents for the DNA-B alleles are: 75(15)

Explanation: The serology and DNA values provided, are validated separately, but also matched. If there is no match between the provided serology and the provided DNA, the record is reported.

HLA/DNA-ERROR: Number of alleles for DRB3/4/5 is more than 2; DRB3/4/5 blanked.

Example: Values are given for DRB4 for FIELD 1 and FIELD 2 and also for DRB5 for FIELD 1

Explanation: Only two allele values are allowed for DRB3, DRB4 and DRB5 combined.

HLA/DNA-ERROR: DRB3 (or DRB4 or DRB5) does not match HLA-DR "values". DRB3 (or DRB4 or DRB5) blanked.

Example: Serology DR is 4 and 11; DRB5 is 01:XX

Explanation: DRB5 is associated with DR2, DR15(2), DR16(2) or DR1(rare). Likewise, DRB3 is associated with DR3, DR5, DR6, DR11(5), DR12(5), DR13(6), DR14(6), DR1403, DR1404, DR17(3), DR18(3); and DRB4 with DR4, DR7, DR9.

Tab Pane | Vectors (Formerly: SP Tab pane)

anchor	728116516
name	Cord blood bank IDs

Cord blood bank IDs

In the XML file format we also defined two fields that are referring to cord blood banks: BANK_MANUF_ID and BANK_DISTRIB_ID.

The BANK_MANUF_ID is the ID corresponding to the cord blood bank that manufactured the cord blood unit (CBU)
The BANK_DISTRIB_ID is the ID corresponding to the cord blood bank that will distribute the CBU

Please find in the table below the ID you have to use for your cord blood banks. The number always consist of 4 digits and is not the same as your ION number. We expect that the BANK_MANUF_ID and the BANK_DISTRIB_ID will be the same for many CBUs.

How to find your ID?

Go to WMDA Share: the following webpage: Database
Find the name of your cord blood bank on this page
- If you can find the name of your cord blood bank, click on the name of your cord blood bank en you will see on the left side in the corner a number (for example: WO-1346); you can use the four digits of this number in the file you are uploading
- If you can not find the name of your cord blood bank, contact the WMDA office at: support@wmda.info

OR

Contatc the WMDA Office at: support@wmda.info

PLEASE NOTE: EMDIS is using very similar fields, but here you need to use a different ID.

Tab Pane | Vectors (Formerly: SP Tab pane)

anchor	640928243
name	Deprecated Code User Guide

Why deprecated code?

WMDA has developed HLA nomenclature guidelines, which have been published in 2007 and 2012. The HLA typing of your donors and cord blood units is validated based on these guidelines. If you list donors/cord blood units, it may happen that you receive the message that the HLA of your donor or cord blood unit is invalid.

There are two forms of ‘deleted’ alleles:

Alleles that have been renamed (e.g. A*01:34N; sequence known to be expressed at low levels and renamed to A*01:01:38L)
Alleles that have been removed without a replacement (e.g. A*2401; sequence shown to contain errors)

What you see in the report?

For data exchange between your organisation and WMDA, it is acceptable to use the older designation for renamed alleles for a period of one year after the renaming. During this grace period, you will receive the following message in your processing report (see below example messages):

#Warning at locus B*: renamed HLA code B*47:01:01:01 is still in grace period, New: 47:01:01:03

And if the deprecated code already passed one year grace period time, you will receive the following message in your processing report:

#Warning at locus B*: deprecated HLA code A*23:ABEBP is now invalid and passed its grace period hence blanked, New: 23:AFVGH 23:AZVXU

What to do with the deprecated code warning?

If you receive such warning messages, you have to update the HLA allele or MAC code within one year. WMDA will not mention the final date of the grace period in the processing report. You can find this information on: http://hla.alleles.org/alleles/deleted.html.

WMDA will provide you advice on how to replace the code. It may be that there are several options possible to update the allele or MAC code. WMDA recommends to perform the replacement using rules as following:

Always pick the same replacement code for a given deprecated code
A possible sophisticated picking strategy is to use the code with the shortest definition string.
For example: if you can choose between 15:01 and 15:01N, you pick the latter. The fewer items without trailing expression character in the definition string the better. Prefer generic codes over specific codes.
Generally, definition strings containing items with trailing Q should be avoided (if possible) as alleles with expression character Q are in danger of being renamed.
For example: in case of B*13:08Q you pick: B*13:08.
If you do not know, go for simple alphanumeric sorting

For 2018 the following alleles were deleted:
• April 2018: B*47:01:01:01 replaced by B*47:01:01:03
• July 2018: B*56:55:01:01 replaced by B*56:55:01:02
• August 2018: A*02:17:01 replaced by A*02:17:02

2019 Update

With the recent HLA Nomenclature Release 3.35.0, the allele HLA-C*03:99 has been renamed to HLA-C*01:169. While renaming of alleles usually does not affect the first two fields of an allele name, this does and as a consequence affects the HLA haplotype frequencies (HF). In fact, we use this allele for the HF sets of DE (1 haplotype) and East Asia (eas, 15 haplotypes). The affected haplotypes have a cumulated frequency of around 1 copy for each of the two HF sets.

We have one abroad patient with that HLA-C*03:99 in the Search&Match database for whom a HLA-C mismatched donor was requested in 2017.

Summary:
1. The allele is generally very rare.
2. Therefore the effect on patients can be assessed as negligible.
3. ZKRD will replace the allele in the HF sets before it expires.

In case you need any support, we recommend to contact the WMDA at: support@wmda.info.

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Key

#

XML file format

1. Introduction

2. XSD schema files

2.1 InventoryType elements

2.2 ItemBaseType elements (for Donors and CBUs)

2.3 hlaType elements

2.4 kirType elements

2.5 idmType elements

2.6 donItemType elements

2.7 cbuItemType elements

2.8 matType elements

#

Minimal required data

#

XML example files

Validation of your XML files

Viewing large files

Generate XML file from excel data source

#

File names

#

How to compress your XML file with ZIP

Creating a compressed zip file in Windows

Creating a compressed zip file in OS X

Creating a compressed zip file in Linux

#

How to encrypt your XML file

STEP 1: Encryption program

STEP 2: Import the public key

STEP 3: Encrypt XML or ZIP file with the public key

#

Explanation of Errors and Warnings in your processing report

Business validation rules applied

File Errors

Record Errors

HLA/DNA Related Errors

Cord blood bank IDs

How to find your ID?

Why deprecated code?

What you see in the report?

What to do with the deprecated code warning?