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Dermadry

by Dermadry Laboratories Inc. Canada EUDAMED

Ref FPRD-053Model Dermadry - Underrams - EN/FR/DE/SP/IT/NL Europe

EMDN Z120604

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-87706700003400 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 22 Oct 2026

Model / Reference
Dermadry - Underrams - EN/FR/DE/SP/IT/NL Europe, FPRD-053
Primary DI / UDI-DI
87706700003400
Basic UDI-DI
B-87706700003400
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 133dad93-6f96-4a4e-9835-052115bf5f38 61 fields · synced 22 Oct 2026