CLEANIS
FR-MF-000004677 · France · ARCUEIL
CLEANIS is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 18 |
|---|
Devices declared under this manufacturer
- CAREBAG BABY, protège Pot
- CAREBAG RECHARGE BOCAUX POUR KIT DE RECUEIL DES URINES SUR 24 H
- CAREBAG, KIT DE RECUEIL DES URINES SUR 24 H
- CAREBAG, recharge kit de recueil des urines sur 24h
- Carebag sac vomitoire avec sachet PRO, boîte de 20
- Carebag ® Protège seau, boîte de 20
- Carebag ® Urinal, boîte de 20
- Carebag ® protège WC, boîte de 20
- Carebag ®Pro Urinal Masculin Recyclé avec support 700ml, boite de 12
- Carebag® Protège bassin de lit 500, boîte de 20
- Carebag®Pro Protège Bassin et Seau Recyclé 700ml, boîte de 20
- Gelmax® Tampon Super-absorbant 700ml boîte de 25
Showing 12 of 18 declared devices.
Catalogue references include 6020020, 7711160, 7711180, 7733190, 7831738, 9538534.
European nomenclature codes declared: V0880, V0812.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 18 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 18 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. CLEANIS was not found in either the U.S. or the Canadian register.