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Dermadry

by Dermadry Laboratories Inc. Canada EUDAMED

Ref FPRD-052Model Dermadry - Total - EN/FR/DE/SP/IT/NL Europe

EMDN Z120604

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-87706700001000 Basic UDI-DIDate8 Aug 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Dermadry - Total
Model / Reference
Dermadry - Total - EN/FR/DE/SP/IT/NL Europe, FPRD-052
Primary DI / UDI-DI
87706700001000
Basic UDI-DI
B-87706700001000
EMDN Code
Z120604 Iontophoresis equipment
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CA-MF-000025789
Authorised representative
CEpartner4U NL-AR-000000111

Other devices from Dermadry Laboratories Inc.

See all devices from Dermadry Laboratories Inc. →

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 69e2fd75-a6ab-4363-adf5-8ab3956cb513 61 fields · synced 23 Oct 2026