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Dermkit

by Melatech ApS 2 variants

Ref DERMKIT1

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5700002317DERMKIT19Q Basic UDI-DI 15700002317213UDI-DIDate29 Jun 2026RegisteredStatusWithdrawn No longer placed on the EU market

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  • Withdrawn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European Union — CE/MDR Withdrawn

Specification

EUDAMED

Model / Reference
DERMKIT1
Primary DI / UDI-DI
15700002317213
Basic UDI-DI
5700002317DERMKIT19Q
EMDN Code
Z12040108 Dermatoscopes
Device Class
Class I
Medical Purpose
Dermoscopy system for visual examination of skin lesions

Manufacturer details

EUDAMED SRN
DK-PR-000056324

Other devices from Melatech ApS

Properties

Other properties (1)

  • Sterile: No