FDA device listing
RANDOX IRON (Fe),RANDOX TOTAL IRON BINDING CAPACITY 2 (TIBC_2),RANDOX TOTAL-IRON BINDING CAPACITY (TIBC)
FDA device listing 1694725245 · RANDOX LABORATORIES, LTD.
Key facts
| Proprietary names | RANDOX IRON (Fe),RANDOX TOTAL IRON BINDING CAPACITY 2 (TIBC_2),RANDOX TOTAL-IRON BINDING CAPACITY (TIBC) |
|---|---|
| Owner/operator | RANDOX LABORATORIES, LTD. |
| Owner/operator number | 8020890 |
| Product codes | JMO |
| Device names | JMO - Ferrozine (Colorimetric) Iron Binding Capacity |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.1415 |
| Review panels | Clinical Chemistry |
| Registered establishments | RANDOX LABORATORIES LIMITED |
| Establishment registrations | 3004493545 |
| FEI numbers | 3004493545 |
| 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