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Fluid Thioglycollate Medium

by Društvo Za Trgovinu I Usluge Promedia Doo Kikinda 3 variants

Ref PRM430B250

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number860601877PRM430G4 Basic UDI-DI 08606018771318UDI-DIDate4 Sep 2026RegisteredStatusActive EUDAMED: not on the EU market

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Model / Reference
PRM430B250
Primary DI / UDI-DI
08606018771318
Basic UDI-DI
860601877PRM430G4
EMDN Code
W0104010306 Culture media in bottles
Device Class
Class A

Manufacturer details

EUDAMED SRN
RS-MF-000025992
Authorised representative
Salus Cons Kft. HU-AR-000006177

Other devices from Društvo Za Trgovinu I Usluge Promedia Doo Kikinda

Properties

Other properties (11)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No