Consulting Wallah › Device Explorer › IVD & laboratory › Vimentin IVD, antibody
Device Explorer · FDA GUDID · GMDN 57705

Vimentin 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 the intermediate filament protein vimentin in a clinical specimen.

US‑registered devices73in commercial distribution
Companies10labelers on GUDID
Single‑use21%of device records
Sterile0%labelled sterile
Prescription21%Rx‑only share
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Share of device records

Diagnostic Biosystems, Inc.1419%
Bio Sb, Inc.1216%
Cell Marque Corporation1115%
Biogenex Laboratories912%
Biocare Medical Llc912%
Leica Biosystems Newcastle Ltd57%
Agilent Technologies Singapore Pte Ltd45%
Epitomics Inc.45%

Top labelers

CompanyDevicesShare
Diagnostic Biosystems, Inc.1419%
Bio Sb, Inc.1216%
Cell Marque Corporation1115%
Biogenex Laboratories912%
Biocare Medical Llc912%
Leica Biosystems Newcastle Ltd57%
Agilent Technologies Singapore Pte Ltd45%
Epitomics Inc.45%
Sakura Finetek U.S.A., Inc.45%
Ventana Medical Systems, Inc.11%

Company = labeler of record on GUDID. 10 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

FLEX Mono Mo A-Vimentin Cl V9 RTU (Dako Omnis)FLEX Mono Mo A-Vimentin Cl V9 RTUFLEX Mono Mo A-Vimentin Cl V9 RTU (Link)Mono Mo A-Vimentin Cl Vim 3B4NovocastraBONDBOND™Novocastra™CONFIRM Anti-Vimentin [V9] Primary AntibodyAnti-VimentinVimentinDiagnostic BioSystemsVimentin (V9) Mouse Monoclonal AntibodyVimentin (EP21) Rabbit Monoclonal Primary AntiboANTI-VIMENTINAnti-VIMENTIN

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 Kits65
NJTIMMUNOHISTOCHEMISTRY REAGENTS AND KITS11

GMDN & GCC registration

  • GMDN code 57705 · non‑implantable
  • Single‑use 21% · sterile 0% · Rx‑only 21% · 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) · 15

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

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

73 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Vimentin IVD, antibody", from 10 companies. The largest labeler is Diagnostic Biosystems, Inc. with 19% of records.

Which FDA product codes apply?

NJT (Immunohistochemistry Reagents And Kits), NJT (IMMUNOHISTOCHEMISTRY REAGENTS AND KITS)

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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