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Adhesive Plaster

by Firstar Healthcare Company Limited (Guangzhou)

Ref OUC-BD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69422726J1.02.60SX Basic UDI-DI 06942272664839UDI-DIDate21 Oct 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
OUC-BD
Primary DI / UDI-DI
06942272664839
Basic UDI-DI
69422726J1.02.60SX
EMDN Code
M9099 General and specialist medical devices – other (suture patches see h900102)
Device Class
Class I
Medical Purpose
22 Pflaster (Standard)； 2 Gelenkpflaster； 8 Pflaster (klein)； 2 Fingerkuppenpflaster； 5 XL-Pflaster； 2 wasserfeste Pflaster

Manufacturer details

EUDAMED SRN
CN-PR-000037943

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Properties

Other properties (1)

  • Sterile: No