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Agar Cu Bila, Azida Si Esculina

by Sc Medicamed Market SRL 5 variants

Ref M1503.800

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 Number594065202M1503800RD Basic UDI-DI 05940652020092UDI-DIDate6 Aug 2024RegisteredStatusActive

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  • Withdrawn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

Device Name
Agar Cu Bila, Azida Si Esculina
Model / Reference
M1503.800
Primary DI / UDI-DI
05940652020092
Basic UDI-DI
594065202M1503800RD
EMDN Code
W0104010306 Culture media in bottles
Device Class
Class A
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
RO-MF-000002243

Other devices from Sc Medicamed Market SRL

See all devices from Sc Medicamed Market SRL →

Properties

  • Professional Testing

Other properties (10)

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