Ahlstrom Germany GmbH
DE-MF-000026936 · Germany · Bärenstein
Ahlstrom Germany GmbH is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Most frequent device types declared: CE-Specimen Collection Card.
Devices declared under this manufacturer
- TFN-Specimen Collection Card
Catalogue references include 8.460.0001.A-Q Rev.8, 8.460.0004.A-N Rev.4, 8.460.0012.A-N Rev.2, 8.460.0038.A-N Rev.4, 8.460.0071.A-N Rev. 1, 8.460.0074.A-Q Rev. 0.
European nomenclature codes declared: W050299.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | AHLSTROM GERMANY GMBH (DE) · FDA 3011213695 |
| Devices in EUDAMED | 7 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| 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. Ahlstrom Germany GmbH is registered in the United States but was not found in the Canadian register.