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Cederroth First Aid Refill to Cederroth First Aid Station

by Orkla Wound Care AB

Ref 51011039

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7340210502004Q Basic UDI-DI 07310800030385UDI-DIDate22 Jun 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  • Withdrawn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
PP 502 Procedure Packs_ Single use Class IIa
Model / Reference
51011039
Primary DI / UDI-DI
07310800030385
Basic UDI-DI
7340210502004Q
EMDN Code
V0501 Clinical emergency kits
Device Class
Class IIa
Medical Purpose
Assortments of products to be used in First Aid situations.

Manufacturer details

EUDAMED SRN
SE-PR-000021131

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Properties

Other properties (1)

  • Sterile: No