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Cormay Crp Ultra

by PZ CORMAY Spółka Akcyjna

Ref 6-300, 4-276Model CORMAY CRP ULTRA, CORMAY CRP ULTRA CALIBRATORS

Active European Union

CE IVDD

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-05907514663002 Basic UDI-DI Date18 Jul 2025RegisteredStatusActive

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  • Withdrawn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/IVDD Active

Specification

EUDAMED

Trade Name
Cormay Crp Ultra
Cormay Crp Ultra Calibrators
Device Name
Crp Ultra
Crp Ultra Calibrators
Model / Reference
CORMAY CRP ULTRA, 6-300, CORMAY CRP ULTRA CALIBRATORS, 4-276
Primary DI / UDI-DI
05907514663002, 05907514642762
Basic UDI-DI
B-05907514663002, B-05907514642762
EMDN Code
W01021109, W0102152210
Device Class
Class IVD General
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000023053

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Properties

  • Human Tissues NoEUDAMEDYesEUDAMED
  • Animal Tissues YesEUDAMEDNoEUDAMED
  • Reagent
  • Professional Testing

Other properties (6)

  • Sterile: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No