FDA device listing
cobas omni ProcessingPlate
FDA device listing 1028031969 · Weidmann Tecnologia Electrica de Mexico S.A. de C.V.
Key facts
| Proprietary names | cobas omni ProcessingPlate |
|---|---|
| Owner/operator | Weidmann Tecnologia Electrica de Mexico S.A. de C.V. |
| Owner/operator number | 10079866 |
| 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 | WEIDMANN TECNOLOGIA ELECTRICA DE MEXICO S.A. DE C.V. |
| Establishment registrations | 3013267051 |
| FEI numbers | 3013267051 |
| Establishment operations | Contract 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