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Skinitril kožní roztok na fibromy, moluska, kondylomata

by ENEO Pharmaceuticals s. r. o.

Ref V-0711

Active European Union

CE MDR

Valid until

9 Dec 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier 3EC International a.s.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859407127SKIT3 Basic UDI-DI 08594071270711UDI-DIDate28 Aug 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2026-MDR/QS-056 Active

    Quality management system EU MDR

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Skinitril
Model / Reference
V-0711
Primary DI / UDI-DI
08594071270711
Basic UDI-DI
859407127SKIT3
Direct Marketing DI
08594071270711
EMDN Code
V0999 Fluids/gases for clinical/therapeutical use - other
Device Class
Class IIa
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000017906

Other devices from ENEO Pharmaceuticals s. r. o.

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