FDA device listing
Centrifuge 5702; Centrifuge 5702 R; Centrifuge 5702 RH
FDA device listing 1251735617 · Eppendorf SE
Key facts
| Proprietary names | Centrifuge 5702; Centrifuge 5702 R; Centrifuge 5702 RH |
|---|---|
| Owner/operator | Eppendorf SE |
| Owner/operator number | 8010471 |
| Product codes | JQC |
| Device names | JQC - Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2050 |
| Review panels | Clinical Chemistry |
| Registered establishments | Eppendorf Manufacturing Corporation, EPPENDORF SE, Eppendorf Zentrifugen GmbH |
| Establishment registrations | 8010471, 3005332796, 3011544811 |
| FEI numbers | 5833, 3005332796, 3011544811 |
| Establishment operations | Contract Manufacturer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database