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medEctoin® Vaginal Gel

by bitop medical GmbH EUDAMED

Active European Union

Ref 38056Model EIC01

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426252692EICPP8D Basic UDI-DIDate5 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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.

Specification

EUDAMED

Model / Reference
EIC01, 38056
Primary DI / UDI-DI
04262526920408
Basic UDI-DI
426252692EICPP8D
EMDN Code
U0899 Gynaecological devices - other
Device Class
Class IIb
Medical Purpose
The device is indicated for the treatment of dry and irritated vaginal mucosa and symptom reduction of vaginal atrophy, such as dryness, itching and burning. It is indicated for hydration and stabilization of dry and irritated vaginal mucosa. Indicated for adult woman (women aged 18 years and above) only.

Manufacturer details

EUDAMED SRN
DE-PR-000056370

Other devices from bitop medical GmbH

See all devices from bitop medical GmbH →

Properties

Other properties (1)

  • Sterile: No