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REPADINA crème

by FARMA-DERMA S.r.l. EUDAMED

Withdrawn Not intended for the EU market

Ref 2017

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803259587TF04EH Basic UDI-DIDate4 Aug 2023RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EPT 0477.MDR.22/5021 Issued

    Quality management system EU MDR

    Notified body
    Notified body 0477
    Issued
    20 Dec 2022
    Expires
    19 Dec 2027

Specification

EUDAMED

Device Name
Cicatridina pomata
Model / Reference
2017
Primary DI / UDI-DI
08032595871651
Basic UDI-DI
803259587TF04EH
EMDN Code
M040499 Dressings for wounds, sores and ulcerations - other
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
IT-MF-000020737

Related devices

Category: Negative-pressure wound therapy system foam dressing, non-antimicrobial

Other devices from FARMA-DERMA S.r.l.

See all devices from FARMA-DERMA S.r.l. →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No