AKTORmed GmbH
DE-MF-000006136 · Germany · Neutraubling
AKTORmed GmbH is registered in the European database on medical devices as a manufacturer, with 49 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 49 |
|---|
Among these devices, 40 are declared active.
Devices declared under this manufacturer
- ADAPTER-1
- DEXTER ENDOSCOPE ARM
- ENDOFIX exo
- JOYSTICK-LH-IIA
- JOYSTICK-LH-IIS
- JOYSTICK-LH-US
- JOYSTICK-RH-IIS
- MOUNT-2A
- PROBE PIN
- TENSION SLEEVE D10
- TROLLEY
- UNIVERSAL JOINT
Showing 12 of 49 declared devices.
Catalogue references include 141362, 161822, 171894, 171943, 202428, 212518.
European nomenclature codes declared: Z1202018099, Z1202018002, Z12029080,Z129080, Z1202018001, S010401, Z12029099,Z129010.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | AKTORmed GmbH (DE) · FDA 3011390076 |
| Devices in EUDAMED | 49 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 49 |
|---|---|
| Found in the U.S. device database | 38 |
| Share | 77.6 % |
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. AKTORmed GmbH is registered in the United States but was not found in the Canadian register.