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Dermkit

by Melatech ApS 2 variants

Ref DERMKIT2

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

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 Number5700002317DERMKIT29S Basic UDI-DI 15700002317206UDI-DIDate29 Jun 2026RegisteredStatusActive

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  • Withdrawn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 Active

Specification

EUDAMED

Device Name
DERMKIT2
Model / Reference
DERMKIT2
Primary DI / UDI-DI
15700002317206
Basic UDI-DI
5700002317DERMKIT29S
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

Properties

Other properties (1)

  • Sterile: No