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Kolodium forte

by ENEO Pharmaceuticals s. r. o. EUDAMED

Active European Union

Ref V-0100

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859407127KFYT Basic UDI-DIDate28 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 2026-MDR/QS-055 Issued

    Quality management system EU MDR

    Notified body
    3EC International a.s. 2265
    Issued
    7 Aug 2026
    Expires
    9 Dec 2027
  • 2026-MDR/TD-055 Issued

    Technical documentation EU MDR

    Notified body
    3EC International a.s. 2265
    Issued
    7 Aug 2026
    Expires
    9 Dec 2027

Specification

EUDAMED

Device Name
Kožní roztok na bradavice
Model / Reference
V-0100
Primary DI / UDI-DI
08594071270100
Basic UDI-DI
859407127KFYT
Direct Marketing DI
08594071270100
EMDN Code
V0999 Fluids/gases for clinical/therapeutical use - other
Device Class
Class III
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000017906

Other devices from ENEO Pharmaceuticals s. r. o.

Properties

  • Incorporates Medicinal Product

Other properties (12)

  • 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