Skip to content

Vidermina MD CLX Single-dose Vaginal Lavage

by ISTITUTO GANASSINI S.p.A. di Ricerche Biochimiche

Ref I50V06490Model sale unit, 5 bottles

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-I50V06490GV Basic UDI-DI D-I50V06490GVUDI-DIDate24 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Vidermina MD CLX Lavanda Vaginale Monodose Export
Model / Reference
sale unit, 5 bottles, I50V06490
Primary DI / UDI-DI
D-I50V06490GV
Basic UDI-DI
B-I50V06490GV
EMDN Code
U0803 Vaginal devices in the form of solutions/creams/ova/tablets
Device Class
Class IIa
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
IT-MF-000027942

Other devices from ISTITUTO GANASSINI S.p.A. di Ricerche Biochimiche

See all devices from ISTITUTO GANASSINI S.p.A. di Ricerche Biochimiche →

Properties

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