FDA device listing
NexSys PCS with Persona PLUS Technology
FDA device listing 1409121939 · Sanmina Corporation
Key facts
| Proprietary names | NexSys PCS with Persona PLUS Technology |
|---|---|
| Owner/operator | Sanmina Corporation |
| Owner/operator number | 2129538 |
| Product codes | GKT |
| Device names | GKT - Separator, Automated, Blood Cell, Diagnostic |
| Device class | Class II |
| Classification regulations (21 CFR) | 864.9245 |
| Review panels | Hematology |
| Registered establishments | Sanmina-SCI Systems (Malaysia) Sdn Bhd |
| Establishment registrations | 3007923088 |
| FEI numbers | 3007923088 |
| Establishment operations | Contract 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