FROXIMUN AG
DE-MF-000014501 · Germany · Schlanstedt
FROXIMUN AG is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Most frequent device types declared: TOXAPREVENT HALISTOP, TOXAPREVENT MEDI PLUS 10 Sachets, TOXAPREVENT MEDI PLUS 10 Sticks, TOXAPREVENT MEDI PLUS 30 Sachets, TOXAPREVENT MEDI PLUS 30 Sticks.
Devices declared under this manufacturer
- TOXAPREVENT HALISTOP
- TOXAPREVENT MEDI PLUS 10 Sachets
- TOXAPREVENT MEDI PLUS 10 Sticks
- TOXAPREVENT MEDI PLUS 30 Sachets
- TOXAPREVENT MEDI PLUS 30 Sticks
- TOXAPREVENT MEDI PLUS ECOLINE 90 g Pulver
- TOXAPREVENT MEDI PURE 180 Capsules
- TOXAPREVENT MEDI PURE 180 Kapslen
- TOXAPREVENT MEDI PURE 60 Capsules
- TOXAPREVENT MEDI PURE 60 Kapseln
- TOXAPREVENT MEDI PURE ECOLINE 180 Kapseln
Catalogue references include 11001041, 11001050, 11001051, 11001053, 11001064, 11201017.
European nomenclature codes declared: G0401, V9017.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. FROXIMUN AG was not found in either the U.S. or the Canadian register.