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Columbia 5% Sheep Blood Agar Plate

by Društvo Za Trgovinu I Usluge Promedia Doo Kikinda 3 variants

Ref PRM144BV60

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE IVDR, withdrawn

Ended

Withdrawn

Date not published (CE IVDR)

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number860601877PRM144BNE Basic UDI-DI 08606018770915UDI-DIDate24 Oct 2023RegisteredStatusWithdrawn No longer placed 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  • Withdrawn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European Union — CE/IVDR Withdrawn

Specification

EUDAMED

Model / Reference
PRM144BV60
Primary DI / UDI-DI
08606018770915
Basic UDI-DI
860601877PRM144BNE
EMDN Code
W0104010499 Prepared media in plates - other
Device Class
Class A
EU market of registration
Bulgaria

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

  • Animal Tissues

Other properties (10)

  • Sterile: No
  • Human 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