FDA device listing
LIAISON Calprotectin Stool Extraction Device,LIAISON Cuvettes on Tray (X0053),LIAISON Reaction Modules (319130),LIAISON…
FDA device listing 1971549117 · DiaSorin Inc.
Key facts
| Proprietary names | LIAISON Calprotectin Stool Extraction Device,LIAISON Cuvettes on Tray (X0053),LIAISON Reaction Modules (319130),LIAISON XL Cuvettes (X0016),LIAISON XL Disposable Tips (X0015 and X0055) |
|---|---|
| Owner/operator | DiaSorin Inc. |
| Owner/operator number | 9051149 |
| Product codes | LXG |
| Device names | LXG - Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2050 |
| Review panels | Clinical Chemistry |
| Registered establishments | DIASORIN INC. |
| Establishment registrations | 2182595 |
| FEI numbers | 2182595 |
| Establishment operations | Specification Developer |
| 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