RECK-Technik GmbH & Co. KG
DE-MF-000005730 · Germany · Betzenweiler
RECK-Technik GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 30 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 30 |
|---|
Among these devices, 30 are declared active.
Devices declared under this manufacturer
- MOTOmed gracile
- MOTOmed layson
- MOTOmed loop
- MOTOmed muvi
Showing 12 of 30 declared devices.
Catalogue references include 260.010, 260.039, 260.040, 260.060, 260.110, 261.030.
European nomenclature codes declared: Z12069099.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | RECK-TECHNIK GMBH & CO. KG (DE) · FDA 9681904 |
| Devices in EUDAMED | 30 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 30 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | RECK TECHNIK GMBH & CO. KG |
North American profile: Both markets. RECK-Technik GmbH & Co. KG is registered in both the United States and Canada.