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LHL medium førstehjelpspute rød

by LHL, Landsforeningen for hjerte, lunge og hjerneslag

Ref 30003

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 Number709005451LHLFA03A3 Basic UDI-DI 07090054510351UDI-DIDate5 Oct 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  • Withdrawn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
30003
Primary DI / UDI-DI
07090054510351
Basic UDI-DI
709005451LHLFA03A3
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
Medical Purpose
First aid kit, non-medicated

Manufacturer details

EUDAMED SRN
NO-PR-000050372

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Properties

Other properties (1)

  • Sterile: No