MTW - Endoskopie W. Haag KG
DE-MF-000004993 · Germany · Wesel
MTW - Endoskopie W. Haag KG is registered in the European database on medical devices as a manufacturer, with 186 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 175 |
|---|---|
| Class IIb | 11 |
Among these devices, 186 are declared sterile, 37 reusable, 11 active.
Devices declared under this manufacturer
- Biopsiezange, \
- ERCP-Katheter
- ERCP-Katheter, filiform
- ERCP-Katheter, wiederverwendbar
- Führungsdraht
- Führungsdraht, \
- Injektionsnadel, doppellumig
- Papillotom, Nadel
- Papillotom, \
- Sprühkatheter
- Steinfänger
- Steinfänger, Nitinol
Showing 12 of 186 declared devices.
Catalogue references include 004126, 004446, 03114634, 990130101, 990130711, 99021281.
European nomenclature codes declared: G0305010201, G0380, G0305010202, G0304010103, P058001, L031301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 186 |
| 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 | 186 |
|---|---|
| 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. MTW - Endoskopie W. Haag KG was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1484GB448260522 | supplemented | 2027-07-01 |