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First Aid Kit

by Yiwu Ori-Power Medtech Co., Ltd. 477 variants

Ref OP703Model 54230

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 Number0697468605FAK25423001RB Basic UDI-DI 06942509210754UDI-DIDate8 May 2024RegisteredStatusActive

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  • Withdrawn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
54230, OP703
Primary DI / UDI-DI
06942509210754
Basic UDI-DI
0697468605FAK25423001RB
EMDN code
M9099 General and specialist medical devices – other (suture patches see h900102)
Device class
Class I
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
Provide first aid

Manufacturer details

EUDAMED SRN
CN-PR-000039035

Other devices from Yiwu Ori-Power Medtech Co., Ltd.

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Properties

Other properties (2)

  • Supplied sterile: No
  • Sterilise before use: No