BEVISTON GmbH
DE-MF-000015203 · Germany · Wurster Nordseeküste
BEVISTON GmbH is registered in the European database on medical devices as a manufacturer, with 35 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 35 |
|---|
Devices declared under this manufacturer
- Bevisto W1 1 Liter Flasche
- Bevisto W1 200 Liter Fass
- Bevisto W2 1 Liter Flasche
- Bevisto W2 10 Liter Kanister
- BevistoCryl plus 1 Liter Flasche
- BevistoCryl plus 10 Liter Kanister
- BevistoCryl plus Wipes 12 x Nachfüllbeutel mit je 120 Tüchern
- BevistoSept plus 1000 Liter IBC
- BevistoSept plus 12 x 1 Liter Flasche
- BevistoSept plus 200 Liter Fass
- BevistoSept plus Wipes 12 x Dose mit je 120 Tüchern
- BevistoSept plus Wipes Dose mit 120 Tüchern
Showing 12 of 35 declared devices.
Catalogue references include 2008, 2013, 2090, 2092, 2100, 3121.
European nomenclature codes declared: V0799, D99, D0701, D0899.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 35 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 35 |
|---|---|
| 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. BEVISTON GmbH was not found in either the U.S. or the Canadian register.