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Cederroth First Aid Burn Kit

by Orkla Wound Care AB

Ref 51011013

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 Number7340210501004K Basic UDI-DI 07310610021801UDI-DIDate29 May 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  • Withdrawn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 501 Procedure Packs_Reusable Class IIa
Model / Reference
51011013
Primary DI / UDI-DI
07310610021801
Basic UDI-DI
7340210501004K
EMDN Code
V0501 Clinical emergency kits
Device Class
Class IIa
Medical Purpose
Assortments of products to be used in First Aid situations, packed in mobile kits, dispensers or first aid stations.

Manufacturer details

EUDAMED SRN
SE-PR-000021131

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Properties

Other properties (1)

  • Sterile: No