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Norgesplaster Scankvikk bandasje 20 x 9, 7 cm

by Orkla Wound Care AB

Ref 510000859

Expiring European Union

CE MDR

Valid until

7 Feb 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

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 Number28620123341-03 Date20 Aug 2026IssuedStatusExpiring expires 7 Feb 2027

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 28620123341-03 Expiring Supplemented Expires in 99 days

    Quality management system EU MDR

    Issued
    20 Aug 2026
    Expires
    7 Feb 2027
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Expiring

Specification

EUDAMED

Device Name
Td 19
Model / Reference
510000859
Primary DI / UDI-DI
07070866033149
Basic UDI-DI
7310610019003Y
EMDN Code
M04010101 Non-woven adhesive dressings, with absorbent pad
Device Class
Class I
EU market of registration
Norway

Manufacturer details

EUDAMED SRN
SE-MF-000021041

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Properties

  • Sterile
  • Contains Latex

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No