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Seguna Sensitive Lady Maxi Night 20 Pz.

by S.I.Cell S.p.A. EUDAMED

Active European Union

Ref AE22302/36076Model LIGHT INCONTINENCE

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805614960LIGHTINCOML Basic UDI-DIDate30 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
LIGHT INCONTINENCE, AE22302/36076
Primary DI / UDI-DI
08056149602973
Basic UDI-DI
805614960LIGHTINCOML
Unit of Use DI
08056149603611
EMDN Code
T0499 Incontinence devices - other
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
IT-MF-000029406

Other devices from S.I.Cell S.p.A.

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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