FDA device listing
GeneChip System 3000Dx v.2
FDA device listing 1074170264 · Life Technologies
Key facts
| Proprietary names | GeneChip System 3000Dx v.2 |
|---|---|
| Owner/operator | Life Technologies |
| Owner/operator number | 9066102 |
| Premarket submissions | DEN040012 |
| Product codes | NSU |
| Device names | NSU - Instrumentation For Clinical Multiplex Test Systems |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.2570 |
| Review panels | Clinical Chemistry |
| Registered establishments | AFFYMETRIX, INC., LIFE TECHNOLOGIES HOLDINGS PTE LTD |
| Establishment registrations | 3003314809, 3010286073 |
| FEI numbers | 3003314809, 3010286073 |
| Establishment operations | Contract Manufacturer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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