Schuchmann GmbH & Co. KG
DE-MF-000013435 · Germany · Bissendorf
Schuchmann GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 239 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 239 |
|---|
Most frequent device types declared: Tina (2025 onwards).
Among these devices, 18 are declared active.
Devices declared under this manufacturer
- Activity Chair UG
- dynamic pacer OR
- dynamic pacer UG
- dynamic pacer mini
- hts UG
- malte
- marcy
- mobile stander
- momo motion dreirad
- prone stander
- sascha
- sofie
Showing 12 of 239 declared devices.
Catalogue references include 33 02 207, 33 04 200, 36 05 000, 49 04 000, 72 00 400, 76 00 100.
European nomenclature codes declared: Y180918, Y050202, Y050201, Y091203, Y121806, Y120606.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | SCHUCHMANN GMBH & CO. KG (DE) · FDA 3017004793 |
| Devices in EUDAMED | 239 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 239 |
|---|---|
| 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: United States only. Schuchmann GmbH & Co. KG is registered in the United States but was not found in the Canadian register.