MEDIWISS ANALYTIC GmbH Gesellschaft für angewandte in-vitro Analytik
DE-MF-000004992 · Germany · Moers
MEDIWISS ANALYTIC GmbH Gesellschaft für angewandte in-vitro Analytik is registered in the European database on medical devices as a manufacturer, with 161 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- CCD-blocking solution
- Panel 1
- Panel 10 Pedi-A
- Panel 11 IT
- Panel 20 LEB RESP-A
- Panel 2B Holz
- Panel 3
- Panel 3 EGY
- Panel 30 Food JORD
- Panel 30 Mix A
- Panel 30 Mix MAG
- Panel 30 Resp BAK
Showing 12 of 161 declared devices.
Catalogue references include 0001, 0016, 0071, 0144, 0295, 0314.
European nomenclature codes declared: W01020205, W01029003.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 161 |
| 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 | 161 |
|---|---|
| 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. MEDIWISS ANALYTIC GmbH Gesellschaft für angewandte in-vitro Analytik was not found in either the U.S. or the Canadian register.