FDA device listing
Sofia 2 Flu + SARS Antigen FIA
FDA device listing 1525544052 · QuidelOrtho Corporation
Key facts
| Proprietary names | Sofia 2 Flu + SARS Antigen FIA |
|---|---|
| Owner/operator | QuidelOrtho Corporation |
| Owner/operator number | 2024674 |
| Product codes | QMN |
| Device names | QMN - Covid-19 Multi-Analyte Antigen Device |
| Device class | Not classified |
| Classification regulations (21 CFR) | ORCA1.QMN |
| Review panels | Microbiology |
| Registered establishments | Ortho-Clinical Diagnostics, Inc., QUIDEL CORP. |
| Establishment registrations | 2024674, 3021090658, 3033751096 |
| FEI numbers | 2024674, 3021090658, 3033751096 |
| Establishment operations | Complaint File Establishment, Specification Developer, 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