FDA device listing
BRUCELLA ABORTUS AND BRU,BRUCELLA ABORTUS AND BRUCELLA MELITENSIS ANTIGENS,ROSE BENGAL ANTIGEN
FDA device listing 1925606521 · CENOGENICS CORPORATION
Key facts
| Proprietary names | BRUCELLA ABORTUS AND BRU,BRUCELLA ABORTUS AND BRUCELLA MELITENSIS ANTIGENS,ROSE BENGAL ANTIGEN |
|---|---|
| Owner/operator | CENOGENICS CORPORATION |
| Owner/operator number | 2243923 |
| Product codes | GSO |
| Device names | GSO - Antigens (Febrile), Agglutination, Brucella Spp. |
| Device class | Class II |
| Classification regulations (21 CFR) | 866.3085 |
| Review panels | Microbiology |
| Registered establishments | CENOGENICS CORP. |
| Establishment registrations | 2250030 |
| FEI numbers | 2250030 |
| 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