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Klinion® Kliniderm® Super fiber + Antimicrobial Polymer Technology™

by Polaroid Therapeutics AG 4 variants

Ref 40511816Model Fiber_20

Active European Union

CE MDR

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number764032807FIBER_20S6 Basic UDI-DI 07640328070366UDI-DIDate29 Apr 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
POLTX_Fiber 200 gsm (Pad), 5x5 cm
Model / Reference
Fiber_20, 40511816
Primary DI / UDI-DI
07640328070366
Basic UDI-DI
764032807FIBER_20S6
EMDN Code
M040404 Cellulose and/or modified cellulose dressings, non-combined or combined with other substances
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000049447
Authorised representative
Qualrep Services B.V. NL-AR-000000537

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Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No