KOSAN PHARMA GmbH
AT-MF-000038337 · Austria · Seewalchen am Attersee
KOSAN PHARMA GmbH is registered in the European database on medical devices as a manufacturer, with 54 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 54 |
|---|
Most frequent device types declared: Mucolaxx® Hustenlöser, Mucolaxx® Hustenlöser junior, Stilaxx® Hustenpastillen, Stilaxx® Hustenpastillen junior, Stilaxx® Hustenstiller.
Devices declared under this manufacturer
- Mucolaxx® Hustenlöser
- Mucolaxx® Hustenlöser junior
- Stilaxx® Hustenpastillen
- Stilaxx® Hustenpastillen junior
- Stilaxx® Hustenstiller
- Stilaxx® Hustenstiller junior
- Tantills® Halspastillen Blackcurrant
- Tantills® Halspastillen HoneyLemon
- Tantills® Halspastillen junior
Showing 12 of 54 declared devices.
Catalogue references include 09120050100152, 09120050100183, 09120050100268, 09120050100435, 09120050103405, 09120050103634.
European nomenclature codes declared: V9017.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 54 |
| Country of registration | Austria |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 54 |
|---|---|
| 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. KOSAN PHARMA GmbH was not found in either the U.S. or the Canadian register.