Pharmazeutische Fabrik Montavit Ges.m.b.H.
AT-MF-000001620 · Austria · Absam
Pharmazeutische Fabrik Montavit Ges.m.b.H. is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 3 |
|---|---|
| Class I | 7 |
Most frequent device types declared: 8,5 g.
Among these devices, 10 are declared sterile.
Devices declared under this manufacturer
- Cathejell Lidocain C
- Glissen C con Lidocaina
Catalogue references include 400824, 400825, 400826, 400829, 400831, 400832.
European nomenclature codes declared: V9007.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | PHARMAZEUTISCHE FABRIK MONTAVIT GES.M.B.H. (AT) · FDA 3008751375 |
| Devices in EUDAMED | 10 |
| Country of registration | Austria |
Device-level evidence
| Devices with a numeric GTIN | 10 |
|---|---|
| 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: United States only. Pharmazeutische Fabrik Montavit Ges.m.b.H. is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
50197-61-B0-00 | issued | 2031-06-09 |
50197-60-00-01 | issued | 2026-11-21 |