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First Aid Kit

by Yiwu Ori-Power Medtech Co., Ltd. 472 variants

Ref ENFAK20200105Model 02001

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 Number69425092FAK202001GQ Basic UDI-DI 06942509212901UDI-DIDate3 Mar 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  • Withdrawn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
02001, ENFAK20200105
Primary DI / UDI-DI
06942509212901
Basic UDI-DI
69425092FAK202001GQ
EMDN Code
M9099 General and specialist medical devices – other (suture patches see h900102)
Device Class
Class I
Medical Purpose
Provide first aid

Manufacturer details

EUDAMED SRN
CN-PR-000039035

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Properties

Other properties (1)

  • Sterile: No