FDA device listing
TECHNICON RA-1000 SYSTEM
FDA device listing 1228518744 · SIEMENS HEALTHCARE DIAGNOSTICS INC.
Key facts
| Proprietary names | TECHNICON RA-1000 SYSTEM |
|---|---|
| Owner/operator | SIEMENS HEALTHCARE DIAGNOSTICS INC. |
| Owner/operator number | 9096044 |
| Product codes | JJF |
| Device names | JJF - Analyzer, Chemistry, Micro, For Clinical Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2170 |
| Review panels | Clinical Chemistry |
| Registered establishments | Siemens Healthcare Diagnostics Inc. |
| Establishment registrations | 2432235 |
| FEI numbers | 2432235 |
| Establishment operations | Complaint File Establishment, Specification Developer |
| 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