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Resistell MicroPrep Kit

by Resistell AG 2 variants

Ref Resistell MicroPrep Kit 50Model Resistell MicroPrep Kit

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 Number7649998169MicroPrepTM Basic UDI-DI 07649998169097UDI-DIDate14 Sep 2026RegisteredStatusActive

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  • Withdrawn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
Resistell MicroPrep Kit, Resistell MicroPrep Kit 50
Primary DI / UDI-DI
07649998169097
Basic UDI-DI
7649998169MicroPrepTM
Direct Marketing DI
07649998169097
EMDN Code
W0104010805 Buffers
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000039090
Authorised representative
Veranex Germany GmbH DE-AR-000005578

Other devices from Resistell AG

Properties

  • Reagent
  • Professional Testing
  • New Device

Other properties (8)

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