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Damor Line ovuli

by Farmaceutici Damor S.p.A.

Ref MDR/08

Damor Line ovuli (MDR/08) is a medical device (EU MDD Class IIa; EMDN category vaginal devices in the form of solutions/creams/ova/tablets) made by Farmaceutici Damor S.p.A., registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-08059777870851), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08059777870851 Basic UDI-DI Date6 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
MDR/08
Primary DI / UDI-DI
08059777870851, 08059777870868
Basic UDI-DI
B-08059777870851, B-08059777870868
EMDN code
U0803 Vaginal devices in the form of solutions/creams/ova/tablets
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000023738

Similar devices in this category

Other devices filed under VAGINAL DEVICES IN THE FORM OF SOLUTIONS/CREAMS/OVA/TABLETS.

Other devices from Farmaceutici Damor S.p.A.

See all devices from Farmaceutici Damor S.p.A. →

Properties

Other properties (12, all answered No)