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Cdmn Selective Supplement SR0173E

by Oxoid Limited

Ref SR0173E

Cdmn Selective Supplement SR0173E is a device classified as IVD General (EU), Class I (US) made by Oxoid Limited, registered in EUDAMED on 24 Aug 2026 (Basic UDI-DI B-05032384012367) and listed in FDA GUDID since 2 Dec 2022 (UDI-DI 05032384012367), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE IVDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD EUDAMED NumberB-05032384012367 Basic UDI-DI 05032384012367UDI-DIDate24 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05032384012367 UDI-DI Date2 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-05032384012367 registered 24 Aug 2026 Active
  • FDA GUDID UDI-DI 05032384012367 listed 2 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05032384012367
  2. Registered EUDAMED B-05032384012367

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/IVDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Cdmn Sel.supplement EUDAMED
Cdmn Selective Supplement GUDID
Generic name
Culture medium antimicrobial supplement IVD
Model / reference
SR0173E
Primary DI / UDI-DI
05032384012367
Basic UDI-DI
B-05032384012367
FDA product code
JSK
EMDN code
W0104010104 Additives for dcm (growth supplements, selective agents, ...)
GMDN term
Culture medium antimicrobial supplement IVD
Device class
Class IVD General EUDAMED
Class I GUDID
Regulation number
866.2450
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IVD General
GUDID
Class I

Device class is stated on each registry's own scale: Class IVD General in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Culture medium antimicrobial supplement IVD

Similar devices in this category

Other devices filed under DEHYDRATED CULTURE MEDIA (DCM - BACTERIOLOGY)).

Other devices from Oxoid Limited

See all devices from Oxoid Limited →

Properties

  • Reagent
  • Professional testing
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)