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eakin perform™ förtjockningsmedel - 60 Sachets

by TG Eakin Limited EUDAMED

Active European Union

Ref SE839020Model eakin peform™

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number050562768PERFORMMK Basic UDI-DIDate21 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Adhesive Remover
Model / Reference
eakin peform™, SE839020
Primary DI / UDI-DI
05060267415240
Basic UDI-DI
050562768PERFORMMK
EMDN Code
A108099 Accessory devices for abdominal ostomy - other
Device Class
Class I
Market of Registration
Sweden

Manufacturer details

EUDAMED SRN
XI-MF-000006712

Other devices from TG Eakin Limited

See all devices from TG Eakin Limited →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: 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