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Aluderm 60 ml Hydrogel

by CF Pharma Ireland Ltd Ireland EUDAMED

Ref FP1947Model Effigerm Wound Care Hydrogel EMDN V9099

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05391525738017 Basic UDI-DIDate3 Mar 2025RegisteredStatusActive

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  • Withdrawn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 22 Oct 2026

Device Name
Aluderm 60ml Hydrogel
Model / Reference
Effigerm Wound Care Hydrogel, FP1947
Primary DI / UDI-DI
05391525738017
Basic UDI-DI
B-05391525738017
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
IE-MF-000004595

Other devices from CF Pharma Ireland Ltd

See all devices from CF Pharma Ireland 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 bdfe0eca-34f6-4e11-a8f8-9cf560b74a13 61 fields · synced 22 Oct 2026