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Wound Plaster

by Ningbo Tianbo First Aid Product Co., Ltd. 4 variants

Ref Rule 1

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697471270TBCKT1P2 Basic UDI-DI 06974712702344UDI-DIDate26 Nov 2024RegisteredStatusActive

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  • Withdrawn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
Wound Plaster
Model / Reference
Rule 1
Primary DI / UDI-DI
06974712702344
Basic UDI-DI
697471270TBCKT1P2
EMDN Code
M0599 Medical plasters - other
Device Class
Class I
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
CN-MF-000016721
Authorised representative
Prolinx GmbH DE-AR-000005129

Other devices from Ningbo Tianbo First Aid Product Co., Ltd.

See all devices from Ningbo Tianbo First Aid Product Co., Ltd. →

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