Johnson & Johnson Medical GmbH
DE-MF-000007714 · Germany · Norderstedt
Johnson & Johnson Medical GmbH is registered in the European database on medical devices as a manufacturer, with 44 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 10 |
|---|---|
| Class IIa | 34 |
Most frequent device types declared: ABSOLOK Clip Applier (for Open Surgery), ABSOLOK Endoscopic Clip Applier, Powerstar.
Among these devices, 44 are declared reusable, 10 active.
Devices declared under this manufacturer
- ABSOLOK
- ENDOPATH
- ETHICON
- LIGACLIP
- POWERSTAR
Showing 12 of 44 declared devices.
Catalogue references include AC107, AP3010S, BP120, BP360, BP720, LC210.
European nomenclature codes declared: L020801, L180201, L020802, L1204, L1205, L0408020305.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Johnson & Johnson MEDICAL GmbH (DE) · FDA 3002294946 |
| Devices in EUDAMED | 44 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 44 |
|---|---|
| Found in the U.S. device database | 3 |
| Share | 6.8 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | JOHNSON & JOHNSON MEDICAL INC. |
North American profile: Both markets. Johnson & Johnson Medical GmbH is registered in both the United States and Canada.