Zimmer Switzerland Manufacturing GmbH
CH-MF-000008793 · Switzerland · Winterthur
Zimmer Switzerland Manufacturing GmbH is registered in the European database on medical devices as a manufacturer, with 78 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 78 |
|---|
Among these devices, 78 are declared reusable.
Authorised representative in the Union: Biomet Global Supply Chain Center B.V..
Devices declared under this manufacturer
- MS-30 Cemented Hip Stem Instruments
- Multi System Instruments - Hips (WIN)
Showing 12 of 78 declared devices.
Catalogue references include 01.00001.014, 01.00359.236, 01.00359.301, 01.01519.227, 6836, 6898.
European nomenclature codes declared: L091104, L091199, L091102, L090403, L091101, L090999.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 78 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 78 |
|---|---|
| Found in the U.S. device database | 17 |
| Share | 21.8 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | ZIMMER SWITZERLAND MANUFACTURING GMBH |
What it holds in Canada
| Licences on record | 55 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 41 |
| Class 3 devices | 14 |
| First licensed | 1999-09-07 |
Licence types: Device Family (29), System (16), Single Device (10).
Licensed under: FEMORAL HEAD FOR TOTAL HIP PROSTHESIS(C0CR), WAGNER REVISION SL STEM, CLS STEM, LOW PROFILE CUP, CLS SPOTORNO STEM RASPS, S.L. REVISION STEM REAMERS.
North American profile: Canada only. Zimmer Switzerland Manufacturing GmbH holds a Canadian licence but was not found in the U.S. register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
MDR 743795 | restricted | 2031-04-28 |