Nitto Advanced Film Gronau GmbH
DE-MF-000031681 · Germany · Gronau
Nitto Advanced Film Gronau GmbH is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Devices declared under this manufacturer
- Mund-Nasen-Schutz Professional Black Typ IIR
- Mund-Nasen-Schutz Professional Med Typ IIR
- Mund-Nasen-Schutz Professional Plus TYP II
Catalogue references include 2EL00150, 3EL00110, 3EL00150, 3EL00310, 3EL00350.
European nomenclature codes declared: T020604.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. Nitto Advanced Film Gronau GmbH was not found in either the U.S. or the Canadian register.