Schneider Medical GmbH
DE-MF-000005484 · Germany · Rheinau
Schneider Medical GmbH is registered in the European database on medical devices as a manufacturer, with 98 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 98 |
|---|
Most frequent device types declared: Einmal-Sofortkompressen Kalt, Einmal-Sofortkompressen Warm 13x15 cm, Mehrfachkompressen heiß/kalt.
Devices declared under this manufacturer
- BodyPal®
- EcoFlex
- Enraf
- Erraff
- FLEXXUM
- FLEXXUM®
- Farmalastic
- Fortacold
- KUDDLER®
- Mehrfachkompresse Kalt/Warm 42x38 cm
- Mehrfachkompresse Kalt/Warm 42x38 cm 6 Stück
- SEIJOS®
Showing 12 of 98 declared devices.
Catalogue references include 046AB, 050AB, 050AB-03, 050B-03, 057A, 057A-01.
European nomenclature codes declared: Z12069099, Z120602.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 98 |
| 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 | 98 |
|---|---|
| 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. Schneider Medical GmbH was not found in either the U.S. or the Canadian register.