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Blødningskontroll Pro 110

by LHL, Landsforeningen for hjerte, lunge og hjerneslag

Ref 25546

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 Number70900545125546LQ Basic UDI-DI 07090054510313UDI-DIDate16 Jun 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  • Withdrawn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
25546
Primary DI / UDI-DI
07090054510313
Basic UDI-DI
70900545125546LQ
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
Medical Purpose
Assortments of products to be used in First Aid situations.

Manufacturer details

EUDAMED SRN
NO-PR-000050372

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Properties

Other properties (1)

  • Sterile: No