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Plan Lila

by Rfsu Ab

Ref 05709556758438

Expiring European Union

CE MDR

Valid until

8 Mar 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number28620129092-01 Date11 Mar 2026IssuedStatusExpiring expires 8 Mar 2027

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Expiring

Specification

EUDAMED

Device Name
Natural Rubber Male Latex Condom
Model / Reference
05709556758438
Primary DI / UDI-DI
05709556758438
Basic UDI-DI
731057Condoms8C
EMDN Code
U110101 Condoms
Device Class
Class IIb
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
SE-MF-000008574

Other devices from Rfsu

See all devices from Rfsu →

Properties

  • Contains Latex

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: 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