Intensiv Medical Products IMPROMEDIFORM GmbH
DE-MF-000014610 · Germany · Lüdenscheid
Intensiv Medical Products IMPROMEDIFORM GmbH is registered in the European database on medical devices as a manufacturer, with 611 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 611 |
|---|
Most frequent device types declared: M01027, M01071, M02056, M03034, M03075.
Among these devices, 611 are declared sterile.
Catalogue references include M10102, M14053, M16085, M17161, M18038, M19059.
European nomenclature codes declared: A03020101, A03040199, A03020102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 611 |
| 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 | 611 |
|---|---|
| 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. Intensiv Medical Products IMPROMEDIFORM GmbH was not found in either the U.S. or the Canadian register.