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SenSura Mio Convex

by Coloplast A/S EUDAMED

Active European Union

Ref 16471

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number57089322975969L Basic UDI-DIDate22 Jun 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  • Withdrawn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

Device Name
SenSura Mio Convex flex ostomy baseplate
Model / Reference
16471
Primary DI / UDI-DI
05708932893602
Unit of Use DI
05708932894432
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
DK-MF-000025526

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