Allmed Medical GmbH
DE-MF-000007862 · Germany · Pulsnitz
Allmed Medical GmbH is registered in the European database on medical devices as a manufacturer, with 155 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 155 |
|---|
Among these devices, 154 are declared sterile.
Devices declared under this manufacturer
- Allmed SafeFlow
Showing 12 of 155 declared devices.
Catalogue references include AV/204, AV/292+B, AV/837/838, AV/837/838PS, AV/T-03/1, KS815/816/BVS/N.
European nomenclature codes declared: F020199, A010499, F01080201, Z12011301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 155 |
| 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 | 155 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | ALLMED MEDICAL GMBH |
What it holds in Canada
| Licences on record | 2 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 1 |
| Class 3 devices | 1 |
| First licensed | 2010-11-03 |
Licence types: Device Family (2).
Licensed under: ALLMED POLYETHERSULFONE DIALYZERS (BIOREMA, QU, ALLMED BLOOD TUBING SET (FOR HEMODIALYSIS).
North American profile: Canada only. Allmed Medical GmbH holds a Canadian licence but was not found in the U.S. register.