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Histology Wax

by Poth Hille & Co 41 variants

Ref Paraffin Wax with added polymer 55-58°C

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number506002325PHCHWXK Basic UDI-DI 05060023251631UDI-DIDate13 May 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  • Withdrawn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
Histology Wax
Model / Reference
Paraffin Wax with added polymer 55-58°C
Primary DI / UDI-DI
05060023251631
Basic UDI-DI
506002325PHCHWXK
EMDN Code
W01030704 Embedding media (histology/cytology)
Device Class
Class A
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
GB-MF-000010882
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Poth Hille & Co

See all devices from Poth Hille & Co →

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