Ackermann Instrumente GmbH
DE-MF-000005479 · Germany · Rietheim-Weilheim
Ackermann Instrumente GmbH is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 5 |
|---|---|
| Class IIb | 1 |
Among these devices, 1 are declared sterile, 1 active.
Catalogue references include 11-1260, 11-1260-5, 11-1263UR, 13-1301DDI, 13-1641UR, 13-1643UR.
European nomenclature codes declared: L181003, K0201010602.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ACKERMANN INSTRUMENTE GMBH (DE) · FDA 8010273 |
| Devices in EUDAMED | 6 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | ACKERMANN INSTRUMENTE GMBH |
North American profile: Both markets. Ackermann Instrumente GmbH is registered in both the United States and Canada.