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If-Norse-Ifak

by AP services A/S

Ref IF-NORSE-IFAK

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5715177Prod-EmergencyJK Basic UDI-DI 05715177032055UDI-DIDate4 Mar 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Emergency
Model / Reference
IF-NORSE-IFAK
Primary DI / UDI-DI
05715177032055
Basic UDI-DI
5715177Prod-EmergencyJK
EMDN Code
Z1399 Non-specific consumables for diagnostic instruments - other
Device Class
Class III
Medical Purpose
The kit is intended for use by trained first responders, police, military personnel, or civilians with basic first aid training.

Manufacturer details

EUDAMED SRN
DK-PR-000041278

Other devices from AP services A/S

Properties

Other properties (1)

  • Sterile: No