bess pro gmbh
DE-MF-000006209 · Germany · Berlin
bess pro gmbh is registered in the European database on medical devices as a manufacturer, with 124 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 83 |
|---|---|
| Class IIa | 41 |
Most frequent device types declared: bess|rhino Thermo-Splint.
Among these devices, 118 are declared sterile, 83 implantable.
Devices declared under this manufacturer
- aerstent GWA
- aerstent TBJ
- aerstent TBS
- aerstent TBY
- aixstent BDP
- aixstent BDS
- aixstent CRE
- aixstent DUS
- aixstent GWG
- aixstent OEC
- aixstent OEL
- aixstent OES
Showing 12 of 124 declared devices.
Catalogue references include 103-28-120, 312-10-080, 503-10-030, 503-14-020, 503-18-050, 522-18-040.
European nomenclature codes declared: P0401, M04040701, P050199, P0502, P0503, Q0399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 124 |
| 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 | 124 |
|---|---|
| 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. bess pro gmbh was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1000310118 | issued | 2031-07-01 |
1000301888 | supplemented | 2030-02-27 |