Ritter GmbH
DE-MF-000036772 · Germany · Schwabmünchen
Ritter GmbH is registered in the European database on medical devices as a manufacturer, with 53 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- Conductive tips H 1000 µL filter
- Conductive tips HT2 1000 µL filter
- Conductive tips HT2 300 µL filter
- Conductive tips HT2 50 µL filter
- Conductive tips QG 50 µL filter
- Conductive tips T 1000 µL DP
- Conductive tips T 1000 µL WB
- Conductive tips T 200 µL DP
- Conductive tips T 200 µL filter
- Conductive tips T 50 µL
- Conductive tips T 50 µL DP
- Conductive tips T 50 µL filter
Showing 12 of 53 declared devices.
Catalogue references include 49002-0000, 49003-0000, 49006-0000, 49009-0115, 49026-0006, 49027-0007.
European nomenclature codes declared: W0503020202, W0503020201.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | RITTER GMBH (DE) · FDA 3001856801 |
| Devices in EUDAMED | 53 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 53 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
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. Ritter GmbH is registered in the United States but was not found in the Canadian register.