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Cicatridina óvulos vaginales

by FARMA-DERMA S.r.l. EUDAMED

Active European Union

Ref 2048

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803259587TF01EB Basic UDI-DIDate5 Jun 2023RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EPT 0477.MDR.22/5019 Issued

    Quality management system EU MDR

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

Specification

EUDAMED

Device Name
Cicatridina Ovuli Vaginali
Model / Reference
2048
Primary DI / UDI-DI
08032595871880
Basic UDI-DI
803259587TF01EB
EMDN Code
U0803 Vaginal devices in the form of solutions/creams/ova/tablets
Device Class
Class IIb
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
IT-MF-000020737

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

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

Properties

Show 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