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AnatoPath Advanced Plast, Premium Histology Paraffin Wax

by AnatoPath Limited

Ref COP/26/0/001.8.1

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 Number5065019469COP260001R6 Basic UDI-DI 05065019469007UDI-DIDate25 Jan 2024RegisteredStatusActive

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  • Withdrawn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
AnatoPath Advanced Plast, Premium Histology Paraffin Wax
Model / Reference
COP/26/0/001.8.1
Primary DI / UDI-DI
05065019469007
Basic UDI-DI
5065019469COP260001R6
Direct Marketing DI
05065019469007
EMDN Code
W01030799 Histology / cytology reagents - other
Device Class
Class A
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
UK-MF-000039624
Authorised representative
Yvsolab NV BE-AR-000039509

Other devices from AnatoPath Limited

Properties

  • Reagent

Other properties (10)

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