Skip to content

Hektoen Enteric Agar

by G. PAPANIKOLAOU & CO. LP - Bioprepare EUDAMED

Active European Union

Ref 010047Model HEKTOEN ENTERIC AGAR 010047

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number52120377010047C5 Basic UDI-DIDate20 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Model / Reference
HEKTOEN ENTERIC AGAR 010047, 010047
Primary DI / UDI-DI
05212037701330
Basic UDI-DI
52120377010047C5
EMDN Code
W0104010405 Non-chromogenic media (plates)
Device Class
Class A
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
EL-MF-000055282

Other devices from G. PAPANIKOLAOU & CO. LP - Bioprepare

See all devices from G. PAPANIKOLAOU & CO. LP - Bioprepare →

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