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Urgo Durable

by Urgo Healthcare Products Co., Ltd 4 variants

Ref 8851401003372

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, self-declared

Class I: no certifier involved

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/MDR Number8851401UHPTF0019G Basic UDI-DI 08851401003372UDI-DIDate9 Jun 2023RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Urgodurable
Model / Reference
8851401003372
Primary DI / UDI-DI
08851401003372
Basic UDI-DI
8851401UHPTF0019G
EMDN Code
M04010199 Adhesive dressings, with absorbent pad - other
Device Class
Class I

Manufacturer details

EUDAMED SRN
TH-MF-000029677
Authorised representative
Compliance Management Solutions Europe LTD BG-AR-000020809

Other devices from Urgo Healthcare Products Co., Ltd

See all devices from Urgo Healthcare Products Co., Ltd →

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