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Heimdall Rescue Bleeding Control Kit Medium

by Ferno Norden Group AS

Ref 5020253

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 Number709007348HEIMBCKEY Basic UDI-DIDate25 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body 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  • Withdrawn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
Heimdall Rescue Bleeding Control Kit
Model / Reference
5020253
Primary DI / UDI-DI
07090073480000
Basic UDI-DI
709007348HEIMBCKEY
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
Medical Purpose
To provide rapid access to selected first response products for emergency bleeding control and immediate first aid response in public areas, workplaces, vehicles, institutions, and other locations where urgent intervention may be required.

Manufacturer details

EUDAMED SRN
NO-PR-000053833

Other devices from Ferno Norden Group AS

Properties

Other properties (1)

  • Sterile: No