Skip to content

first aid kit

by GAUKE Healthcare Co., Ltd 125 variants

Ref /

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69514547305V8 Basic UDI-DI 06951454728146UDI-DIDate20 Mar 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  • Withdrawn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

Model / Reference
/
Primary DI / UDI-DI
06951454728146
Basic UDI-DI
69514547305V8
EMDN Code
V9012 Non-specialist surgical instruments and kits, single-use
Device Class
Class I
Medical Purpose
For temporary treatment in case of accidental injury.

Manufacturer details

EUDAMED SRN
CN-PR-000038433

Other devices from Gauke Healthcare Co., Ltd

See all devices from Gauke Healthcare Co., Ltd →

Properties

  • Sterile