Pereg GmbH
DE-MF-000048645 · Germany · Waldkraiburg
Pereg GmbH is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Devices declared under this manufacturer
- HemoCheck-S
- HydroCheck-E
- Pyromol-E
- Pyromol-Test
- SonoCheck
- TOSI
- TOSI-FlexiCheck
- TOSI-LumCheck
Catalogue references include 11100-12, 20100-25, 20240-25, 30550-30, 67067-12, 67070-20.
European nomenclature codes declared: Z12011301, Z12019080, Z12029080, Z12011302.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. Pereg GmbH was not found in either the U.S. or the Canadian register.