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Cederroth First Aid/ Salvequick Plaster dispenser

by Orkla Wound Care AB

Ref 490700

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7340210501000PL Basic UDI-DI 07310614907002UDI-DIDate22 May 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  • Withdrawn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

Device Name
PP 501 Procedure Packs_Reusable Class I and Is
Model / Reference
490700
Primary DI / UDI-DI
07310614907002
Basic UDI-DI
7340210501000PL
EMDN Code
V0501 Clinical emergency kits
Device Class
Class I
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