Ritter Implants GmbH & Co. KG
DE-MF-000006414 · Germany · Biberach
Ritter Implants GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 895 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 895 |
|---|
Most frequent device types declared: Cortical drills, Dental Drills and Surgical Kits, Dental Tools, Impression Copings, Laboratory Analogs.
Among these devices, 3 are declared sterile, 111 reusable, 213 with a measuring function.
Devices declared under this manufacturer
- Ritter
Showing 12 of 895 declared devices.
Catalogue references include CDEP-2.8-16, CDEP-5.4-11.5, IA-PUT-SW, PA-CF-NC30, RDS-ASC-D7, RT-45TSQ.
European nomenclature codes declared: P01020180, P01020101.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Ritter Implants GmbH & Co. KG (DE) · FDA 3009528809 |
| Devices in EUDAMED | 895 |
| Country of registration | Germany |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | RITTER IMPLANTS GMBH & CO. KG |
What it holds in Canada
| Licences on record | 4 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 3 |
| Class 3 devices | 1 |
| First licensed | 2019-03-15 |
Licence types: Device Family (2), Device Group Family (1), System (1).
Licensed under: RITTER SURGICAL KITS, RITTER IMPLANTS, RITTER IMPLANT DRILLS, RITTER IMPLANT TOOLS.
North American profile: Both markets. Ritter Implants GmbH & Co. KG is registered in both the United States and Canada.