Molzym GmbH & Co.KG
DE-MF-000037419 · Germany · Bremen
Molzym GmbH & Co.KG 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
Most frequent device types declared: U-010-024, U-010-048, U-050-024, U-050-048, U-120-024.
Devices declared under this manufacturer
- Add-On 10 CE IVD
- Micro-Dx™ CE IVD
- MolYsis-SNplus™ IVD
- SepsiTest™-UMD CE IVD
- UMD-SelectNA™ CE IVD
Catalogue references include U-010-024, U-010-048, U-050-024, U-120-024, U-120-048, U-200-024.
European nomenclature codes declared: W0105900101,W0105900102, W0105900101.
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 | 2 |
|---|---|
| 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. Molzym GmbH & Co.KG was not found in either the U.S. or the Canadian register.