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eakin Release™ Pflasterentferner 50ml

by TG Eakin Limited XI EUDAMED

Ref DE839023Model eakin Release™ EMDN A108005

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number050562768RELEASEHR 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  • Withdrawn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 · synced 25 Oct 2026

Device Name
Adhesive Remover
Model / Reference
eakin Release™, DE839023
Primary DI / UDI-DI
05060267413239
Basic UDI-DI
050562768RELEASEHR
EMDN Code
A108005 Devices for the removal of adhesives from the peristomal skin
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
XI-MF-000006712

Other devices from TG Eakin Limited

See all devices from TG Eakin Limited →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 05060267413239|050562768RELEASEHR 61 fields · synced 25 Oct 2026