Ritex GmbH
DE-MF-000005708 · Germany · Bielefeld
Ritex GmbH is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: Medizinische Schutzhüllen für Ultraschallsonden.
Devices declared under this manufacturer
- Coperture protettive medicali per sonde
- Medicinska hygienskydd för ultraljudssonder
- Medicinske overtræk til ultralydssonder
- Medisinske probetrekk for ultralydsprober
- Medizinische Schutzhüllen für Ultraschallsonden
- Medizinische Schutzhüllen für Ultraschallsonden 34 mm
- Ratiomed
- Ritex Schutzhüllen für Ultraschallsonden
- Sondosecur
- \tMedicinska hygienskydd för ultraljudssonder
- medimex
Showing 12 of 20 declared devices.
Catalogue references include 02728, 0272806, 0273410, 02828, 02851, 02881.
European nomenclature codes declared: T030199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 20 |
|---|---|
| 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: Neither register. Ritex GmbH was not found in either the U.S. or the Canadian register.