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Sign in to claim this brandMurata Vios, Inc.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 700 Commerce Drive, Suite 190, Woodbury, MN, 55125
- Website
- murata.com
- —
- —
- [email protected]
- Phone
- 866-990-1434
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3015328411
- DUNS Number
- 026867345
Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vios Monitoring System Bedside Monitor | BSM2050 Software | FDA UDI | Class II | Active |
| Vios Montioring System Adapter | L2050G Adapter | FDA UDI | Class II | Active |
| Vios Monitoring System Pulse Oximetry Sensor | L2050R Pulse Oximetry Sensor | FDA UDI | Class II | Active |
| Vios Monitoring System Central Server | VCS2050 Software | FDA UDI | Class I | Active |
| Vios Monitoring System Central Station Monitor | CSM2050 Software | FDA UDI | Class I | Active |
| Vios Monitoring System Chest Sensor | CS2050 Chest Sensor | FDA UDI | Class II | Active |
| Vios Monitoring System Mobile Application | VMM2050 Mobile Application | FDA UDI | Class II | Active |
| Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050 | K241728 | FDA 510(k) | Class II | Active |
| Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software | K232354 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Recalls (4)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Aug 9, 2024 | Z-1292-2025 | — | open, classified | Batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet. Depleted batteries may lead to tablet connectivity issues. |
| Apr 22, 2024 | Z-1069-2025 | — | open, classified | During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms can become distorted and will flicker or flash very fast. This issue only occurs on the Central Station Monitor (CSM) in the patient tiles view and is not seen at any other point during patient monitoring & not on the Bedside Monitor. |
| Jun 6, 2023 | Z-1169-2025 | — | open, classified | A premature failure condition was identified with the L2050R pulse oximeter SpO2 sensor that connects to the L2050G Vios chest sensor device. When a failure occurs, a Pulse Ox Sensor Off warning condition will be incorrectly displayed by the system. |
| Jun 21, 2021 | Z-0956-2025 | — | completed | During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms can become distorted and will flicker or flash very fast. This issue only occurs on the Central Station Monitor (CSM) in the patient tiles view and is not seen at any other point during patient monitoring & not on the Bedside Monitor. |