Perpedes GmbH
DE-MF-000006250 · Germany · Lenningen
Perpedes GmbH is registered in the European database on medical devices as a manufacturer, with 3 138 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 3 138 |
|---|
Most frequent device types declared: AA.
Devices declared under this manufacturer
- O2 Bari Light, L 26
- O2 Novara Light, 22
- O2 Vermont Light, R 30
- O5 Bari Light, R 45
- O5 Como Camo Light, L 29
- O5 Florida Light, L 40
- O5 Maine, L 37
- O8 Bari Light, R 40
- O8 Florida Light, L 30
- O8 Maine, L 42
- O8 Oklahoma, R 40
- O8 Pisa, 30
Showing 12 of 3 138 declared devices.
Catalogue references include O2CS330, O5AL240, O5CQ345, O8AL230, O8CO242, O8CQ340.
European nomenclature codes declared: Y063303.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 3 138 |
| 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 | 3 138 |
|---|---|
| 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. Perpedes GmbH was not found in either the U.S. or the Canadian register.