Skip to content

Verbiese

by Laboratoire Verbiese 7 variants

Ref 512302_35, 512029_33, 512029_35_2, 512029_69_1, 512302SOL, 512029_47, 512302_40

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 Number37013999512302SOLPR Basic UDI-DI Date30 Nov 2022RegisteredStatusActive

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  • Withdrawn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
Fixateur AFA en solution
Formol tamponné pbs 4 % en solution
Model / Reference
512302_35, 512029_33, 512029_35_2, 512029_69_1, 512302SOL, 512029_47, 512302_40
Primary DI / UDI-DI
03701399900526, 03701399900854, 03701399900847, 03701399900007, 03701399901134, 03701399900151, 03701399900502
Basic UDI-DI
37013999512302SOLPR, 37013999512029SOLQR
EMDN Code
W01030705 Fixing reagents (histology/cytology)
Device Class
Class A
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000023445

Other devices from Laboratoire Verbiese

See all devices from Laboratoire Verbiese →

Properties

  • Reagent
  • Professional Testing

Other properties (9)

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