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Histology Wax

by Poth Hille & Co 41 variants

Ref Histowax 5457SF 25kg bag

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number506002325PHCHWXK Basic UDI-DI 05060023250276UDI-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  • Withdrawn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
Histowax 5457SF 25kg bag
Primary DI / UDI-DI
05060023250276
Basic UDI-DI
506002325PHCHWXK
EMDN Code
W01030704 Embedding media (histology/cytology)
Device Class
Class A
EU market of registration
Poland

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