Skip to content

Conveen

by Coloplast A/S 27 variants

Ref 050501

Conveen (050501) is a Class I device made by Coloplast A/S, registered in EUDAMED on 16 Sep 2026 (Basic UDI-DI 570893229790295), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number570893229790295 Basic UDI-DI Date16 Sep 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Conveen leg bag strap hooks and loops closure, buttons
Model / reference
050501
Primary DI / UDI-DI
05701780785587, 05701780573740, 05701780572514, 05701780573504, 05701780572491
Basic UDI-DI
570893229790295
Unit of use DI
05708932135184
EMDN code
A0680 Drainage and fluid collection devices - accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Poland
Czechia
Sweden
Austria
France

Manufacturer details

EUDAMED SRN
DK-MF-000025526

Similar devices in this category

Other devices filed under DRAINAGE AND FLUID COLLECTION DEVICES - ACCESSORIES.

Other devices from Coloplast A/S

See all devices from Coloplast A/S →

Properties

Other properties (14, all answered No)