FDA device listing
CF0201001,CF0201002,CF0202003,CF221,CF321,Clinical Centrifuge,MC-6K,MC-7K,Mini Centrifuge,TM-5000
FDA device listing 1781528870 · Guangzhou Four E's Scientific Co., Ltd.
Key facts
| Proprietary names | CF0201001,CF0201002,CF0202003,CF221,CF321,Clinical Centrifuge,MC-6K,MC-7K,Mini Centrifuge,TM-5000 |
|---|---|
| Owner/operator | Guangzhou Four E's Scientific Co., Ltd. |
| Owner/operator number | 10035903 |
| 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 | Guangzhou Four E's Scientific Co., Ltd. |
| Establishment registrations | 3009155756 |
| FEI numbers | 3009155756 |
| 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