Eppendorf SE
DE-MF-000006237 · Germany · Hamburg
Eppendorf SE is registered in the European database on medical devices as a manufacturer, with 69 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- Centrifuge 5420
- Centrifuge 5425
- Centrifuge 5425 R
- Centrifuge 5427R
- Centrifuge 5430
- Centrifuge 5430 R
- Centrifuge 5430R
- Centrifuge 5702
- Centrifuge 5702R
- Centrifuge 5810
- Centrifuge 5810R
- Centrifuge 5910Ri
Showing 12 of 69 declared devices.
Catalogue references include 5405 000.158, 5406 000.011, 5406 000.615, 5428 000.619, 5453 000.011, 5702 000.329.
European nomenclature codes declared: W02069003.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | EPPENDORF SE (DE) · FDA 8010471 |
| Devices in EUDAMED | 69 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 69 |
|---|---|
| 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. Eppendorf SE is registered in the United States but was not found in the Canadian register.