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Apteczka Smaochodowa

by Danyang Sunmed Healthcare Corporation

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, 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 Number697456746000266C Basic UDI-DI 06974567464305UDI-DIDate9 Apr 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  • Withdrawn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

Device Name
First aid kit
Model / Reference
/
Primary DI / UDI-DI
06974567464305
Basic UDI-DI
697456746000266C
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
Medical Purpose
intended for emergency simple treatment of accident.

Manufacturer details

EUDAMED SRN
CN-PR-000047222

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Properties

Other properties (1)

  • Sterile: No