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Vilowond®Nonwoven Non-Sterile

by Pharmaplast 16 variants

Ref VILONWN12-7575

Active European Union

CE MDR

Valid until

24 Nov 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier 3EC International a.s.

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/MDR Number2025-MDR/QS-071 Date24 Nov 2025IssuedStatusActive expires 24 Nov 2030

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2025-MDR/QS-071 Active

    Quality management system EU MDR

    Certifier
    3EC International a.s. 2265
    Issued
    24 Nov 2025
    Expires
    24 Nov 2030

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Vilowond® Gauze & Vilowond® Nonwoven
Model / Reference
VILONWN12-7575
Primary DI / UDI-DI
06221329006991
Basic UDI-DI
62220238VilowondGNWBP
EMDN Code
M0202010101 Non-woven folded gauzes, without x-ray detectable thread, sterile
Device Class
Class I
EU market of registration
Northern Ireland

Manufacturer details

EUDAMED SRN
EG-MF-000004501
Authorised representative
E C REP LIMITED IE-AR-000003995

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Properties

Other properties (13)

  • Sterile: No
  • 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