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Conveen 05050

by Coloplast A/S

Ref 05050

Conveen 05050 is a Class I device made by Coloplast A/S, registered in EUDAMED on 16 Sep 2026 (Basic UDI-DI 570893229790295) and listed in FDA GUDID since 17 Jan 2023 (UDI-DI 05701780574174), active as of 25 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number570893229790295 Basic UDI-DI Date16 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05701780574174 UDI-DI Date17 Jan 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 570893229790295 registered 16 Sep 2026 Active
  • FDA GUDID UDI-DI 05701780574174 listed 17 Jan 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05701780574174
  2. Registered EUDAMED 570893229790295

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Conveen
Generic name
Personal device holder, reusable
Device name
Conveen leg bag strap hooks and loops closure, buttons
Model / Ref / Catalog
05050
Primary DI / UDI-DI
05701780574174 EUDAMED
05701780580168 EUDAMED
05701780572675 EUDAMED
05701780572934 EUDAMED
05701780574105 EUDAMED
05701780894111 EUDAMED
05701780889599 EUDAMED
05701780572651 EUDAMED
05708932252843 EUDAMED
05701780494373 EUDAMED
05701780572590 EUDAMED
05701780866682 EUDAMED
05701780572958 EUDAMED
05708932469814 EUDAMED
05701780573030 EUDAMED
05701780572415 EUDAMED
05701780572521 EUDAMED
05708932135184 GUDID
Basic UDI-DI
570893229790295
Unit of use DI
05708932135184
FDA product code
NNW
EMDN code
A0680 Drainage and fluid collection devices - accessories
GMDN term
Personal device holder, reusable
Device class
Class I
Regulation number
876.5250
EU registration type
Standard device
EU market of registration
Hungary
Germany
Spain
Liechtenstein
Slovakia
Croatia
Estonia
Norway
Romania
Ireland
Slovenia
Finland
Bulgaria
Italy
Portugal
Belgium
GUDID distribution status
In Commercial Distribution
Size
Length — 23.6 Inch
Length — 60 Centimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
05701780574174
05701780580168
05701780572675
05701780572934
05701780574105
05701780894111
05701780889599
05701780572651
05708932252843
05701780494373
05701780572590
05701780866682
05701780572958
05708932469814
05701780573030
05701780572415
05701780572521
GUDID
05708932135184

The registries describe this device under different primary UDI-DIs (EUDAMED lists 05701780574174, 05701780580168, 05701780572675, 05701780572934, 05701780574105; FDA GUDID lists 05708932135184), so their flags are not compared.

Related devices

Category: Personal device holder, reusable

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

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (21, all answered No)