FDA device listing
BioPlex 2200 MMV IgM Calibrator Set,BioPlex 2200 MMV IgM Control Set,BioPlex 2200 MMV IgM Reagent Pack
FDA device listing 1414130791 · BIO-RAD LABORATORIES, INC.
Key facts
| Proprietary names | BioPlex 2200 MMV IgM Calibrator Set,BioPlex 2200 MMV IgM Control Set,BioPlex 2200 MMV IgM Reagent Pack |
|---|---|
| Owner/operator | BIO-RAD LABORATORIES, INC. |
| Owner/operator number | 3022521 |
| Product codes | LFY |
| Device names | LFY - Enzyme Linked Immunoabsorbent Assay, Varicella-Zoster |
| Device class | Class II |
| Classification regulations (21 CFR) | 866.3900 |
| Review panels | Microbiology |
| Registered establishments | BIO-RAD LABORATORIES, INC. |
| Establishment registrations | 3032705 |
| FEI numbers | 3002701146 |
| Establishment operations | U.S. Manufacturer of Export Only Devices |
| 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