FDA device listing
T3-RIA-CT
FDA device listing 1872047579 · DIAsource ImmunoAssays, SA
Key facts
| Proprietary names | T3-RIA-CT |
|---|---|
| Owner/operator | DIAsource ImmunoAssays, SA |
| Owner/operator number | 10037912 |
| Product codes | CDP |
| Device names | CDP - Radioimmunoassay, Total Triiodothyronine |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1710 |
| Review panels | Clinical Chemistry |
| Registered establishments | DiaSource ImmunoAssays, SA |
| Establishment registrations | 3009335633 |
| FEI numbers | 3009335633 |
| 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