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Genio Universal Cassette - White - Taped - 750 Pcs - Suitable for Ir Laser Printing

by Diapath S.p.A. società a socio unico

Ref GC0526Model UNIVERSAL AND BIOPSY GENIO CASSETTE

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number8033895W05030501GenioCsDZ Basic UDI-DI 08033895011761UDI-DIDate18 Jun 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  • Withdrawn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

Device Name
Genio Cassette
Model / Reference
UNIVERSAL AND BIOPSY GENIO CASSETTE, GC0526
Primary DI / UDI-DI
08033895011761
Basic UDI-DI
8033895W05030501GenioCsDZ
Direct Marketing DI
08033895011761
EMDN Code
W05030501 Inclusion devices, cassettes
Device Class
Class A
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000027016

From the manufacturer

Manufacturer's product page: Traceability system for biocassettes and slides

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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