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Dermalux

by Aesthetic Technology Ltd United Kingdom EUDAMED

Ref 1000033 EMDN Z12040202

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060762460141 Basic UDI-DIDate15 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Dermalux Flex MD
Model / Reference
1000033
Primary DI / UDI-DI
05060762460141
Basic UDI-DI
B-05060762460141
EMDN Code
Z12040202 Phototherapy equipment
Device Class
Class IIa
Market of Registration
Denmark

Manufacturer details

EUDAMED SRN
GB-MF-000033533
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Aesthetic Technology, Ltd.

See all devices from Aesthetic Technology, Ltd. →

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED d9eb8b31-9b41-4707-853e-2252cbd81833 61 fields · synced 23 Oct 2026