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Anaerobe Blood Agar W/Kanamycin & Vancomycin

by G. PAPANIKOLAOU & CO. LP - Bioprepare

Ref 010220Model ANAEROBE BLOOD AGAR W/KANAMYCIN & VANCOMYCIN 010220

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number52120377010220BT Basic UDI-DI 05212037700043UDI-DIDate19 Oct 2026RegisteredStatusActive

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  • Withdrawn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
ANAEROBE BLOOD AGAR W/KANAMYCIN & VANCOMYCIN 010220, 010220
Primary DI / UDI-DI
05212037700043
Basic UDI-DI
52120377010220BT
EMDN Code
W0104010405 Non-chromogenic media (plates)
Device Class
Class A
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
EL-MF-000055282

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Properties

  • Reagent
  • Professional Testing

Other properties (9)

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