Hupfer Metallwerke GmbH & Co KG
DE-MF-000007652 · Germany · Coesfeld
Hupfer Metallwerke GmbH & Co KG is registered in the European database on medical devices as a manufacturer, with 257 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 257 |
|---|
Most frequent device types declared: Instrumentenfixierungen, Siebkörbe, Siebschalen.
Devices declared under this manufacturer
- De 250/250/016
- De/SiKo 580/270/077
- EiKo 228/245/45 FG
- FIX/Instr R1 SiScha/240 SET
- FIX/Instr R6 SiKo 480
- SiKo NTOC 480/300/060 oR FG LB/SG
- SiKo/Endo 290/080/052 oR oG DS mD 2-fach
- SiKo/Endo 460/080/052 oR oG DS mD
- SiKo/Endo 635/245/099 BR mD
- SiSch 240/254/050 SR FG DM
- SiSch 252/250/120 SR FG DM
- SiSch 410/254/070 SR FG DM
Showing 12 of 257 declared devices.
Catalogue references include 7500001, 7500049, 7501402, 7501414, 7501669, 7501749.
European nomenclature codes declared: S010401.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | HUPFER METALLWERKE GMBH & CO. KG (DE) · FDA 3002259632 |
| Devices in EUDAMED | 257 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 257 |
|---|---|
| Found in the U.S. device database | 5 |
| Share | 1.9 % |
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. Hupfer Metallwerke GmbH & Co KG is registered in the United States but was not found in the Canadian register.