möLab GmbH
DE-MF-000022941 · Germany · Langenfeld
möLab GmbH is registered in the European database on medical devices as a manufacturer, with 47 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- möLab® Cannabinoide Drogen Einzeltest Kassette
- möLab® Gonorrhoe Test
- möLab® Metamphetamine Drogen Einzeltest Streifen
- möLab® OneSecond Multi-Dip Test 10-fach (AMP,BAR,BZD,COC,THC,MET,MTD,M
- möLab® OneSecond Multi-Dip Test 10-fach (AMP,BZD,COC,THC,MET,MTD,MOR,M
- möLab® OneSecond Multi-Dip Test 4-fach (AMP,BZD,COC,MOR)
- möLab® OneSecond Multi-Dip Test 4-fach (AMP,COC,THC,MET)
- möLab® OneSecond Multi-Dip Test 5-fach (AMP, BZD,COC,MOR,EDDP)
- möLab® OneSecond Multi-Dip Test 6-fach (AMP, BZD,COC,THC,MET,MOR)
- möLab® OneSecond Multi-Dip Test 6-fach (BZD,COC,THC,MET,MTD,MOR)
- möLab® OneSecond Multi-Dip Test 8-fach (AMP,BZD,COC,THC,MTD,MOR,BUP,MD
- möLab® Troponin I Test qualitativ
Showing 12 of 47 declared devices.
Catalogue references include 0230002, 0270049, 0270055, 0270062, 0270065, 0270098.
European nomenclature codes declared: W0102160511, W0102160505, W01021306, W0102160501, W0105010201, W0102160502.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 47 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. möLab GmbH was not found in either the U.S. or the Canadian register.