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SenSura Mio Convex

by Coloplast A/S EUDAMED

Active European Union

Ref 18670

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number570893229762898 Basic UDI-DIDate11 Dec 2025RegisteredStatusActive

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  • Withdrawn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 High Output ostomy bag 1-piece convex
Model / Reference
18670
Primary DI / UDI-DI
05708932051767, 05708932065399, 05708932051422, 05701780226554
Basic UDI-DI
570893229762898
Unit of Use DI
05701780152587, 05701780152518, 05701780152617, 05701780226578
EMDN Code
A1001020202 One-piece ileostomy bags for retracted stoma, convex, with tissue cover
Device Class
Class I
Market of Registration
Denmark
Liechtenstein
Netherlands
Czechia

Manufacturer details

EUDAMED SRN
DK-MF-000025526

Other devices from Coloplast A/S

See all devices from Coloplast A/S →

Properties

Show 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