FDA device listing
IntelliVue Patient Monitor,M3014A Capnography Extension,Mainstream CO2 Sensor,Reusable ADU-PED Airway Adapter…
FDA device listing 1818383077 · CEVA Logistics Limited
Key facts
| Proprietary names | IntelliVue Patient Monitor,M3014A Capnography Extension,Mainstream CO2 Sensor,Reusable ADU-PED Airway Adapter, Philips,Reusable NEO Airway Adapter, Philips,Single-Patient Use Adult Airway Adapter |
|---|---|
| Owner/operator | CEVA Logistics Limited |
| Owner/operator number | 10085484 |
| Premarket submissions | K050762 |
| Product codes | MHX |
| Device names | MHX - Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1025 |
| Review panels | Cardiovascular |
| Registered establishments | CEVA LOGISTICS LIMITED |
| Establishment registrations | 3023272766 |
| FEI numbers | 3023272766 |
| Establishment operations | Foreign Exporter |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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