Dräger Safety AG & Co. KGaA
DE-MF-000014172 · Germany · Lübeck
Dräger Safety AG & Co. KGaA is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 4 |
|---|
Among these devices, 2 are declared active, 1 with a measuring function.
Devices declared under this manufacturer
- Dräger Alcotest 7000 med
- Dräger Companion 4me
- Dräger DrugTest 5000
- Dräger DrugTest 5000 Analyzer
- Dräger DrugTest 5000 STK 2 UK
- Dräger DrugTest 5000 STK 5
- Dräger DrugTest 5000 STK 6
- Dräger DrugTest 5000 STK 7
- Mouthpiece Alcomed with valve
- Mouthpiece Alcotest 3820/4000 Companion 4me
Catalogue references include 3705618, 3719512, 8319900, 8323156, 8323439, 8323646.
European nomenclature codes declared: V0380, V030299, W0201020101, W0102090102,W0102090105,W0102090106,W0102090113, W0102090102,W0102090104,W0102090105,W0102090106,W0102090110,W0102090113, W0102090102,W0102090104,W0102090105,W0102090106,W0102090110,W0102090113,W0102090199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| 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 | 10 |
|---|---|
| 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. Dräger Safety AG & Co. KGaA was not found in either the U.S. or the Canadian register.