aap Implantate AG
DE-MF-000005994 · Germany · Berlin
aap Implantate AG is registered in the European database on medical devices as a manufacturer, with 278 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 200 |
|---|---|
| Class IIb | 78 |
Most frequent device types declared: Bone plates (non-sterile), Instrument.
Among these devices, 78 are declared implantable, 200 reusable.
Devices declared under this manufacturer
- LOQTEQ®
Showing 12 of 278 declared devices.
Catalogue references include IC 0006-15, IC 6935-21, IC 6936-02, IC 6980-21, IL 1003-33, IU 7706-50.
European nomenclature codes declared: V0402, P09120503, L098099, V0480.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | AAP IMPLANTATE AG (DE) · FDA 8043862 |
| Devices in EUDAMED | 278 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 278 |
|---|---|
| Found in the U.S. device database | 275 |
| Share | 98.9 % |
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. aap Implantate AG is registered in the United States but was not found in the Canadian register.