Consulting Wallah › Device Explorer › IVD & laboratory › HLA class I antigen tissue typing IVD, kit, multip
Device Explorer · FDA GUDID · GMDN 56324

HLA class I antigen tissue typing IVD, kit, multiplex

A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of one or multiple HLA class I antigens in a clinical specimen, using a multiplex method.

US‑registered devices110in commercial distribution
Companies2labelers on GUDID
Single‑use98%of device records
Sterile0%labelled sterile
Prescription2%Rx‑only share
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Share of device records

Caredx Ab10898%
Immucor Gti Diagnostics, Inc.22%

Top labelers

CompanyDevicesShare
Caredx Ab10898%
Immucor Gti Diagnostics, Inc.22%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

A-B-CHLA-C low ScreeningHLA-Cw*04:09NHLA-C highHLA-C*18HLA-C*17HLA-C*16HLA-C*15HLA-C*14HLA-C*12HLA-C*08HLA-C*07HLA-C*06HLA-C*05HLA-C*04HLA-C*03

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
MZITest,Qualitative,For Hla,Non-Diagnostic4
MZITest, Qualitative, For Hla, Non-Diagnostic1

GMDN & GCC registration

  • GMDN code 56324 · non‑implantable
  • Single‑use 98% · sterile 0% · Rx‑only 2% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

How many hla class i antigen tissue typing ivd, kit, multiplex products are registered in the US?

110 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "HLA class I antigen tissue typing IVD, kit, multiplex", from 2 companies. The largest labeler is Caredx Ab with 98% of records.

Which FDA product codes apply?

MZI (Test,Qualitative,For Hla,Non-Diagnostic), MZI (Test, Qualitative, For Hla, Non-Diagnostic)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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