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Tissue Biopsy Cassette White 1000 Pcs

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

Ref 070345Model TISSUE BIOPSY CASSETTE

Active European Union

CE IVDR

Valid until

No date given

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 Number8033895W0503050107034XQF Basic UDI-DI 08033895018364UDI-DIDate11 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  • Withdrawn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
Tissue Biopsy Cassette
Model / reference
TISSUE BIOPSY CASSETTE, 070345
Primary DI / UDI-DI
08033895018364
Basic UDI-DI
8033895W0503050107034XQF
Direct marketing DI
08033895018364
EMDN code
W05030501 Inclusion devices, cassettes
Device class
Class A
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000027016

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Properties

  • Professional testing

Other properties (12)

  • Supplied sterile: No
  • Sterilise before use: No
  • Contains human tissues or cells: No
  • Contains animal tissues or cells: No
  • Contains substances of microbial origin: No
  • Reagent: No
  • IVD kit: No
  • Self-testing: No
  • Near-patient testing: No
  • Companion diagnostics: No
  • IVD instrument: No
  • New device: No