Consulting Wallah › Device Explorer › IVD & laboratory › MSH2 antigen IVD, antibody
Device Explorer · FDA GUDID · GMDN 57428

MSH2 antigen IVD, antibody

One or multiple immunoglobulins capable of binding to specific antigenic determinants and intended to be used for the qualitative and/or quantitative detection of MSH2 antigen in a clinical specimen.

US‑registered devices62in commercial distribution
Companies11labelers on GUDID
Single‑use23%of device records
Sterile0%labelled sterile
Prescription27%Rx‑only share
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Share of device records

Bio Sb, Inc.1829%
Biocare Medical Llc1321%
Diagnostic Biosystems, Inc.711%
Fuzhou Maixin Biotech Co., Ltd.46%
Agilent Technologies, Inc.46%
Leica Biosystems Newcastle Ltd46%
Epitomics Inc.46%
Biogenex Laboratories35%

Top labelers

CompanyDevicesShare
Bio Sb, Inc.1829%
Biocare Medical Llc1321%
Diagnostic Biosystems, Inc.711%
Fuzhou Maixin Biotech Co., Ltd.46%
Agilent Technologies, Inc.46%
Leica Biosystems Newcastle Ltd46%
Epitomics Inc.46%
Biogenex Laboratories35%
Slmp, Llc23%
Sakura Finetek U.S.A., Inc.23%
Agilent Technologies Singapore Pte Ltd12%

Company = labeler of record on GUDID. 11 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Mouse Monoclonal Anti-Human MSH2(MX061) AntibodyMSH2 IHC pharmDx (Dako Omnis)FLEX Mono Mo A-Hu MSH2, Cl FE11 RTU (Dako Omnis)FLEX Mono Mo A-Hu MutS Protein Homolog 2 Cl FEMono Mo A-Hu MutS Protein Homolog 2 Cl FE11BOND™BONDNovocastraNovocastra™MSH2MSH6 [BC19]Diagnostic BioSystemsIHCANTI-MSH2Rabbit Monoclonal Anti-Human MSH2 Antibody, RED2Tissue-Tek Genie®

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

FDA product codes

CodeNameDevices
NJTImmunohistochemistry Reagents And Kits51
NJTIMMUNOHISTOCHEMISTRY REAGENTS AND KITS11
QNHImmunohistochemistry test, DNA mismatch repair (MMR) Protein1
PZJLynch Syndrome Test System1

GMDN & GCC registration

  • GMDN code 57428 · non‑implantable
  • Single‑use 23% · sterile 0% · Rx‑only 27% · 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

Total Volume (Milliliter) · 16

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

How many msh2 antigen ivd, antibody products are registered in the US?

62 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "MSH2 antigen IVD, antibody", from 11 companies. The largest labeler is Bio Sb, Inc. with 29% of records.

Which FDA product codes apply?

NJT (Immunohistochemistry Reagents And Kits), NJT (IMMUNOHISTOCHEMISTRY REAGENTS AND KITS), QNH (Immunohistochemistry test, DNA mismatch repair (MMR) Protein), PZJ (Lynch Syndrome Test System)

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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