Consulting Wallah › Device Explorer › IVD & laboratory › CD1a cell marker IVD, antibody
Device Explorer · FDA GUDID · GMDN 56922

CD1a cell marker 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 CD1a cell marker in a clinical specimen.

US‑registered devices50in commercial distribution
Companies13labelers on GUDID
Single‑use40%of device records
Sterile0%labelled sterile
Prescription18%Rx‑only share
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Share of device records

Diagnostic Biosystems, Inc.1326%
Cell Marque Corporation612%
Bio Sb, Inc.612%
Fuzhou Maixin Biotech Co., Ltd.48%
Leica Biosystems Newcastle Ltd48%
Sakura Finetek U.S.A., Inc.48%
Biocare Medical Llc36%
Biogenex Laboratories36%

Top labelers

CompanyDevicesShare
Diagnostic Biosystems, Inc.1326%
Cell Marque Corporation612%
Bio Sb, Inc.612%
Fuzhou Maixin Biotech Co., Ltd.48%
Leica Biosystems Newcastle Ltd48%
Sakura Finetek U.S.A., Inc.48%
Biocare Medical Llc36%
Biogenex Laboratories36%
Becton, Dickinson And Company24%
Life Technologies Corporation24%
Agilent Technologies Singapore Pte Ltd12%
Agilent Technologies, Inc.12%

Company = labeler of record on GUDID. 13 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Mouse Monoclonal Anti-Human CD1a(MX115) AntibodyMono Mo A-Hu CD1a/FITC Cl NA1/34FLEX Mono Mo A-Hu CD1a Cl 010 RTU (Link)BONDNovocastraNovocastra™BOND™CD1a [O10]Diagnostic BioSystemsCD1a (EP3622) Rabbit Monoclonal Primary AntibodyCD1a (EP3622) Rabbit Monoclonal AntibodyIHCANTI-CD1ATissue-Tek Genie®HorizonN/A

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 Kits43
MVUReagents, specific, analyte7
NJTIMMUNOHISTOCHEMISTRY REAGENTS AND KITS5
MVUREAGENTS,SPECIFIC,ANALYTE1

GMDN & GCC registration

  • GMDN code 56922 · non‑implantable
  • Single‑use 40% · sterile 0% · Rx‑only 18% · 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) · 7

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

How many cd1a cell marker ivd, antibody products are registered in the US?

50 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "CD1a cell marker IVD, antibody", from 13 companies. The largest labeler is Diagnostic Biosystems, Inc. with 26% of records.

Which FDA product codes apply?

NJT (Immunohistochemistry Reagents And Kits), MVU (Reagents, specific, analyte), NJT (IMMUNOHISTOCHEMISTRY REAGENTS AND KITS), MVU (REAGENTS,SPECIFIC,ANALYTE)

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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