Hydas GmbH & Co. KG
DE-MF-000016598 · Germany · Frankfurt
Hydas GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 19 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 19 |
|---|
Most frequent device types declared: 3031.1.00, 9987.1.01.
Devices declared under this manufacturer
- Beckenboden-Trainer (Norma)
- Beckenbodentrainer SGL
- Geradehalter (Haltungs- und Stützband)
- Inhalationstopf
- Inhalator, mit 2 Mund-Nase-Aufsätzen
- Inkontinenzhose
- Inkontinenzslip für Saugeinlagen
- Orthopädischer Bauch- und Rückenstützgürtel
- Reisestrumpf XL; Schuhgröße 36-38, schwarz
- Spreizfußbandage
- Triggerknopf + rosa Tape
- Triggerknopf ohne Tape
Showing 12 of 19 declared devices.
Catalogue references include 0007.1.38, 1627.1.00, 19460, 3003.1.00, 9681.1.00, 9681.5.00.
European nomenclature codes declared: T0499, T99, R900901, Z120602, M030499, Q0399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 19 |
| 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 | 19 |
|---|---|
| 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. Hydas GmbH & Co. KG was not found in either the U.S. or the Canadian register.