FDA device listing
High speed centrifuge,High speed refrigerated centrifuge,Large capacity refrigerated centrifuge
FDA device listing 1668427599 · AIKANG MEDTECH CO., LTD
Key facts
| Proprietary names | High speed centrifuge,High speed refrigerated centrifuge,Large capacity refrigerated centrifuge |
|---|---|
| Owner/operator | AIKANG MEDTECH CO., LTD |
| Owner/operator number | 10044248 |
| 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 | AIKANG MEDTECH CO., LTD |
| Establishment registrations | 3010402964 |
| FEI numbers | 3010402964 |
| Establishment operations | 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