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FC2 Female Condom

by The Female Health Company (UK) Plc EUDAMED

Active European Union

Ref 290322, 010822, JFU50001, 5111, 020822, 340401.3, 030822, 070323, 1220, JFU30003

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5022213000009HC Basic UDI-DIDate13 May 2024RegisteredStatusActive

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  • Withdrawn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

Device Name
FC2 Female Condom
Model / Reference
290322, 010822, JFU50001, 5111, 020822, 340401.3, 030822, 070323, 1220, JFU30003
Primary DI / UDI-DI
05022213000009, 05022213000078, 05022213000245, 05022213000184, 05022213000085, 05022213000139, 05022213000092, 05022213000207, 05022213000054, 05022213000252
Basic UDI-DI
5022213000009HC
EMDN Code
U110203 Female condoms
Device Class
Class IIb
Market of Registration
France
Spain

Manufacturer details

EUDAMED SRN
GB-MF-000029355
Authorised representative
Advena Limited MT-AR-000000234

Other devices from The Female Health Company (UK) Plc

See all devices from The Female Health Company (UK) Plc →

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