BPR Swiss GmbH
CH-MF-000018810 · Switzerland · Oberdiessbach
BPR Swiss GmbH is registered in the European database on medical devices as a manufacturer, with 19 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 19 |
|---|
Among these devices, 16 are declared active.
Authorised representative in the Union: Klaus Seiler.
Devices declared under this manufacturer
- Combi-Cart Clinic
- Denta-Boy 202
- Denta-Cart 404
- Denta-Cart Clinic
- Denta-Chair 303
- Denta-LED
- Denta-Port 303
- Denta-Vac
- Easy-Port 303
- Master-Vac
- Minimax-Vac
- Smart-Port
Showing 12 of 19 declared devices.
Catalogue references include D-10000, D-11500, D-13100, D-17000, D-18000, D-31000.
European nomenclature codes declared: Z12110101, Z12010702.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 19 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 19 |
|---|---|
| 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. BPR Swiss GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
M.2022.MDR1005 | issued | 2027-07-27 |