Gimmi GmbH
DE-MF-000005445 · Germany · Tuttlingen
Gimmi GmbH is registered in the European database on medical devices as a manufacturer, with 2 741 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 2 741 |
|---|
Among these devices, 2 260 are declared reusable, 10 active.
Devices declared under this manufacturer
- ALPHAARTHRO
- ALPHAHYSTERO
- ALPHALED
- ALPHANOVOCAM
- ALPHAPORT
- ALPHATRAY
- AlphaSMART
- AlphaScope™
Showing 12 of 2 741 declared devices.
Catalogue references include AA.1262.14, AA.1849.18, AD.1078.01, AD.1174.16, QL.3006.11, QO.0540.04.
European nomenclature codes declared: L03140199, L031306, L010403, S010499, L059001, Z12021003.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | GIMMI GMBH (DE) · FDA 9612074 |
| Devices in EUDAMED | 2 741 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 2 741 |
|---|---|
| Found in the U.S. device database | 777 |
| Share | 28.3 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | GIMMI GMBH |
North American profile: Both markets. Gimmi GmbH is registered in both the United States and Canada.