Willy-Rusch GmbH
DE-MF-000020784 · Germany · Kernen im Remstal
Willy-Rusch GmbH is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 15 |
|---|
Most frequent device types declared: 173810-000160, 173810-000180, 173810-000200, 173810-000220, 173810-000240.
Among these devices, 15 are declared sterile.
Devices declared under this manufacturer
- Post OP 3 W Foley catheter, Couvelaire
- Post OP 3 W Foley catheter,cyl.,2 eyes
Showing 12 of 15 declared devices.
Catalogue references include 173810-000160, 173810-000180, 173810-000200, 173810-000220, 173810-000240, 173910-000200.
European nomenclature codes declared: U010201, U010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| 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 | 15 |
|---|---|
| Found in the U.S. device database | 8 |
| Share | 53.3 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | WILLY RUSCH GMBH |
North American profile: Canada only. Willy-Rusch GmbH holds a Canadian licence but was not found in the U.S. register.