MS Westfalia GmbH
DE-MF-000042752 · Germany · Troisdorf
MS Westfalia GmbH is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 5 |
|---|
Among these devices, 5 are declared active, 5 with a measuring function.
Devices declared under this manufacturer
- Jenny Defibrillator Module paddle version
- Jenny Defibrillator Module slim version
- Jenny Monitoring Module
- Jenny Ventilation Module
Catalogue references include 0101.00.00001.000, 0102.00.00000.000, 0103.00.00000.000, 0104.00.00000.000, 0104.00.00001.000.
European nomenclature codes declared: Z12030502, Z1203010504, V9099, Z1203020202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. MS Westfalia GmbH was not found in either the U.S. or the Canadian register.