Philips Intellivue Xds Software
Philips Medizin Systeme Boeblingen
FDA Clearance Information
The Philips IntelliVue XDS Software was cleared through the FDA 510(k) pathway on April 26, 2019. It is manufactured by Philips Medizin Systeme Boeblingen and classified as a Class 2 device under product code MSX.
What It Is
FDA-Cleared Indications
- Display patient-monitoring information from compatible Philips IntelliVue monitoring systems on additional or remote displays.
- Support access to monitoring data in clinical environments where patient information must be viewed from more than one location.
Clinical Applications
- Viewing vital signs and other patient-monitoring parameters at remote clinical workstations.
- Supporting continuous monitoring in intensive care and other hospital settings.
- Displaying monitoring information during perioperative care when compatible Philips IntelliVue systems are in use.
- Providing clinicians with access to patient-monitoring data without requiring them to remain at the primary monitor.
Practical Considerations
- Compatibility must be confirmed with the installed Philips IntelliVue monitors, software versions, network configuration and display hardware.
- The software depends on the hospital information-technology network and appropriate system configuration; network interruptions may affect remote data display.
- It displays monitoring information but does not replace clinical assessment, the primary patient monitor or established alarm-management procedures.
- This is software rather than an implanted or patient-contact device; MRI compatibility is not determined by the software alone. Any computer, display or monitoring hardware used near an MRI scanner must be separately evaluated under the facility's MRI safety policy.
- Training, cybersecurity controls, software updates and verification of displayed patient identity are important before clinical use.
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RCT|prospective|retrospective|case Series|other View Source →Frequently Asked Questions
What is Philips IntelliVue XDS Software used for?
It is used for displaying and managing patient monitoring data across multiple remote screens in clinical settings.
What specialties typically use this device?
Specialties such as critical care, emergency medicine, and anesthesiology commonly use this device.
What are the FDA-cleared indications?
The software is indicated for displaying and managing patient monitoring data, suitable for continuous monitoring in critical care and surgical settings.