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Coloplast Baby

by Coloplast A/S 3 variants

Part of a family of 8 devices: see the family page

Ref 18705

Coloplast Baby (18705) is a Class IIa device made by Coloplast A/S, registered in EUDAMED on 21 Jul 2026 (Basic UDI-DI 570893229760892), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number570893229760892 Basic UDI-DI 05701780265164UDI-DIDate21 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
SenSura Mio Baby flex ostomy baseplate
Model / reference
18705
Primary DI / UDI-DI
05701780265164
Basic UDI-DI
570893229760892
Unit of use DI
05708932736398
EMDN code
A1002010401 Universal plates for abdominal stoma (colo-, ileo-, urostomy) with non-introflex stoma
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
DK-MF-000025526

Similar devices in this category

Other devices filed under ABDOMINAL OSTOMY DEVICES.

Other devices from Coloplast A/S

See all devices from Coloplast A/S →

Properties

Other properties (14, all answered No)