Medz Europe B.V.
NL-MF-000022387 · Netherlands · Ermelo
Medz Europe B.V. is registered in the European database on medical devices as a manufacturer, with 36 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 36 |
|---|
Most frequent device types declared: Eurogloves Soft-Nitrile powder free, Eurogloves Solid Nitrile powder free.
Devices declared under this manufacturer
- Eurofloves Soft-Nitrile powder free black
- Eurogloves Soft Nitrile powder free black
- Eurogloves Soft Nitrile powder free blue
- Eurogloves Solid Nitrile powder free Long Cuff
- Eurogloves Solid Nitrile powder free black
- Eurogloves Solid Nitrile powder free blue
- Eurogloves latex powder free
- Eurogloves vinyl powder free
Showing 12 of 36 declared devices.
Catalogue references include 305010, 305050, 306010, 306020, 306030, 601300.
European nomenclature codes declared: T01020204, T010201, T01020201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 36 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 36 |
|---|---|
| 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. Medz Europe B.V. was not found in either the U.S. or the Canadian register.