FDA device listing
AFIAS ROTA,AFIAS Rota/Adeno
FDA device listing 1972310213 · Boditech Med Inc.
Key facts
| Proprietary names | AFIAS ROTA,AFIAS Rota/Adeno |
|---|---|
| Owner/operator | Boditech Med Inc. |
| Owner/operator number | 10046783 |
| Product codes | LIQ |
| Device names | LIQ - Enzyme Linked Immunoabsorbent Assay, Rotavirus |
| Device class | Class I |
| Classification regulations (21 CFR) | 866.3405 |
| Review panels | Microbiology |
| Registered establishments | BODITECH MED INC. |
| Establishment registrations | 3009491259 |
| FEI numbers | 3009491259 |
| 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