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Cure-Aid® Dermi plaster

by Pharmaplast EUDAMED

Active European Union

Ref DERMIN601000

Overview

Cure-Aid Dermi plaster is a non-sterile, multi-component medical device designed for the treatment of wounds and skin injuries. The device is used to provide sterile dressings for wound care, promoting healing and preventing infection. With its advanced features and rigorous testing protocols, Cure-Aid Dermi plaster has been certified as a Class I medical device by regulatory authorities worldwide.

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number62220238CureAidNSQ7 Basic UDI-DIDate21 Apr 2024RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Cure Aid Non-Sterile Product line
Model / Reference
DERMIN601000
Primary DI / UDI-DI
06223004867569
Basic UDI-DI
62220238CureAidNSQ7
EMDN Code
M030102 Non-woven bandages
Device Class
Class I
Market of Registration
Northern Ireland

Manufacturer details

EUDAMED SRN
EG-MF-000004501
Authorised representative
E C REP LIMITED IE-AR-000003995

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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