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Duboscq-Brasil Picroformalin - 2 Lt

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

Ref P0094Model GENERAL FIXATIVE, SUITABLE FOR BIOPSIES, RTU - DUBOSCQ-BRASIL PICROFORMALIN

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 7 Nov 2026. What this means

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number8033895W01030705DubBra3C Basic UDI-DI 08033895004213UDI-DIDate2 Jul 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  • Withdrawn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
Duboscq-Brasil Picroformalin
Model / reference
GENERAL FIXATIVE, SUITABLE FOR BIOPSIES, RTU - DUBOSCQ-BRASIL PICROFORMALIN, P0094
Primary DI / UDI-DI
08033895004213
Basic UDI-DI
8033895W01030705DubBra3C
Direct marketing DI
08033895004213
EMDN code
W01030705 Fixing reagents (histology/cytology)
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

  • Reagent
  • Professional testing

Other properties (11)

  • 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
  • IVD kit: No
  • Self-testing: No
  • Near-patient testing: No
  • Companion diagnostics: No
  • IVD instrument: No
  • New device: No