FDA device listing
SmartLinx Vitals Plus Patient Monitoring System
FDA device listing 1398109732 · Flash Global
Key facts
| Proprietary names | SmartLinx Vitals Plus Patient Monitoring System |
|---|---|
| Owner/operator | Flash Global |
| Owner/operator number | 10051121 |
| Premarket submissions | K171751 |
| Product codes | DQA, DXN, FLL, MWI |
| Device names | DQA - Oximeter, DXN - System, Measurement, Blood-Pressure, Non-Invasive, FLL - Continuous Measurement Thermometer, MWI - Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1130, 870.2300, 870.2700, 880.2910 |
| Review panels | Cardiovascular, General Hospital |
| Registered establishments | Flash Global |
| Establishment registrations | 3012251275 |
| FEI numbers | 3012251275 |
| Establishment operations | Contract Manufacturer, Manufacturer, Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 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