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DibuCell ACTIVE EXUDATE ACTIVE DRESSING MATERIAL ACCELERATING WOUND HEALING

by Celther Polska Sp. z o.o. 2 variants

Ref DAE

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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/MDD NumberB-05906874713648 Basic UDI-DI 05906874713648UDI-DIDate13 Jul 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
DibuCell ACTIVE EXUDATE AKTYWNY OPATRUNEK PRZYSPIESZAJĄCY GOJENIE RAN
Model / Reference
DAE
Primary DI / UDI-DI
05906874713648
Basic UDI-DI
B-05906874713648
EMDN Code
M040499 Dressings for wounds, sores and ulcerations - other
Device Class
Class III
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000002202

Related devices

Category: Negative-pressure wound therapy system foam dressing, non-antimicrobial

Other devices from Celther Polska Sp. z o.o.

Properties

  • Sterile
  • Animal Tissues

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No