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Centric Cf 108 Gr IVD

by DOMEL, d.o.o. 2 variants

Ref 231.3.500/IVD (230V)Model Laboratory centrifuge

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number383008323CENTRIFUGEWD Basic UDI-DI 03830083230158UDI-DIDate10 Mar 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Model / Reference
Laboratory centrifuge, 231.3.500/IVD (230V)
Primary DI / UDI-DI
03830083230158
Basic UDI-DI
383008323CENTRIFUGEWD
Direct Marketing DI
03830083230158
EMDN Code
W02069005 Refrigerated centrifuges
Device Class
Class A
EU market of registration
Slovenia

Manufacturer details

EUDAMED SRN
SI-MF-000030074

Other devices from DOMEL, d.o.o.

See all devices from DOMEL, d.o.o. →

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