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Mueller Hinton Agar Plate

by Društvo Za Trgovinu I Usluge Promedia Doo Kikinda 2 variants

Ref PRM173V240

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 Number860601877PRM173G7 Basic UDI-DI 08606018770786UDI-DIDate29 Jun 2026RegisteredStatusActive EUDAMED: not 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  • Withdrawn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 Active

Specification

EUDAMED

Model / Reference
PRM173V240
Primary DI / UDI-DI
08606018770786
Basic UDI-DI
860601877PRM173G7
EMDN Code
W0104010403 Susceptibility test media (plates)
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