FDA device listing
CENTRIFUGE
FDA device listing 1806540201 · Ningbo Greetmed Medical Instruments Co., Ltd.
Key facts
| Proprietary names | CENTRIFUGE |
|---|---|
| Owner/operator | Ningbo Greetmed Medical Instruments Co., Ltd. |
| Owner/operator number | 10033128 |
| 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 | NINGBO GREETMED MEDICAL INSTRUMENTS CO., LTD. |
| Establishment registrations | 3008496560 |
| FEI numbers | 3008496560 |
| Establishment operations | Foreign Exporter |
| 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