Consulting Wallah › Device Explorer › IVD & laboratory › Culture medium antimicrobial supplement IVD
Device Explorer · FDA GUDID · GMDN 58556

Culture medium antimicrobial supplement IVD

A culture medium supplement containing one or multiple antimicrobials that is intended to be used to suppress or inhibit the growth of native or resident microorganisms present in a clinical specimen to enhance recovery, isolation, and/or growth of pathogenic

US‑registered devices65in commercial distribution
Companies4labelers on GUDID
Single‑use18%of device records
Sterile0%labelled sterile
Prescription15%Rx‑only share
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Share of device records

Oxoid Limited4874%
Becton, Dickinson And Company1015%
Clark Laboratories, Inc.58%
Remel, Inc.23%

Top labelers

CompanyDevicesShare
Oxoid Limited4874%
Becton, Dickinson And Company1015%
Clark Laboratories, Inc.58%
Remel, Inc.23%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

BartelsXLT-4 Selective SupplementSPUTASOL (LIQUID)CAMPYLOBACTER GROWTH SUPPLEMENT (LIQUID)CHROMOGENIC CANDIDA SELECTIVE SUPPLEMENTSALMONELLA SELECTIVE SUPPLEMENTMODIFIED KARMALI SEL. SUPP.MODIFIED PRESTON CAMPYLOBACTER SUPPORSAB SELECTIVE SUPPLEMENTBURKHOLDERIA CEPACIA SELECTIVE SUPPLEMNOVOBIOCIN SUPPLEMENTCEFIXIME TELLURITE SELECTIVE SUPPLEMENTFILTERED HORSE SERUMEGG YOLK EMULSIONPOTASSIUM TELLURITE 3.5%UREA 40%

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

FDA product codes

CodeNameDevices
JSKSupplement, Culture Media46
MDBSYSTEM, BLOOD CULTURING9
JSJCulture Media, Selective And Non-Differential5
KITMedia And Components, Synthetic Cell And Tissue Culture3
MDBSystem, blood culturing2
MZCSystem, detection, bacterial, for platelet transfusion produ2

GMDN & GCC registration

  • GMDN code 58556 · non‑implantable
  • Single‑use 18% · sterile 0% · Rx‑only 15% · 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) · 9

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

How many culture medium antimicrobial supplement ivd products are registered in the US?

65 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Culture medium antimicrobial supplement IVD", from 4 companies. The largest labeler is Oxoid Limited with 74% of records.

Which FDA product codes apply?

JSK (Supplement, Culture Media), MDB (SYSTEM, BLOOD CULTURING), JSJ (Culture Media, Selective And Non-Differential), KIT (Media And Components, Synthetic Cell And Tissue Culture)

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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