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First Aid Kit

by Dragon Medical Co., Ltd 23 variants

Ref FAKBS

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69424557DWFAKAU2 Basic UDI-DI 06942455708107UDI-DIDate12 Jan 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  • Withdrawn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
FAKBS
Primary DI / UDI-DI
06942455708107
Basic UDI-DI
69424557DWFAKAU2
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
Medical Purpose
Suitable for emergency use before the hospitals, medical rescue, rescue, health services, home, office, school, automobile, outdoor, etc. and medical care in the hospital.

Manufacturer details

EUDAMED SRN
CN-PR-000051403

Other devices from Dragon Medical Co., Ltd

See all devices from Dragon Medical Co., Ltd →

Properties

Other properties (1)

  • Sterile: No