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Selenite F Broth

by Društvo Za Trgovinu I Usluge Promedia Doo Kikinda EUDAMED

Withdrawn Not intended for the EU market

Ref PRM052E25

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number860601877PRM052FS Basic UDI-DIDate4 Sep 2026RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Withdrawn

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Model / Reference
PRM052E25
Primary DI / UDI-DI
08606018771028
Basic UDI-DI
860601877PRM052FS
EMDN Code
W0104010206 Media in tubes (solid & liquid)
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