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16977807313002

by Yiwu Kebon Healthcare Co., Ltd.

Ref 16977807313002Model FAK3001A

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 Number697780731KBCE30LN Basic UDI-DI 16977807313002UDI-DIDate16 Oct 2025RegisteredStatusActive

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  • Withdrawn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
FAK3001A, 16977807313002
Primary DI / UDI-DI
16977807313002
Basic UDI-DI
697780731KBCE30LN
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
Medical Purpose
It is used for dealing with wound in emergency situation

Manufacturer details

EUDAMED SRN
CN-PR-000049556

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Properties

Other properties (1)

  • Sterile: No