OmniWire integrates with IntraSight, Philips' secure interventional applications platform that integrates a comprehensive suite of clinically proven modalities including iFR, FFR, IVUS (intravascular ultrasound) and co-registration [7] to simplify complex interventions and speed routine procedures. With iFR pullback and co-registration, physicians can identify the precise locations causing ischemia, plan stent length and placement with a virtual stent, and predict physiologic improvement.
"With integration and co-registration on our IntraSight platform, measurement with iFR, and now enhanced wire performance thanks to OmniWire, we're providing clinicians with an advanced solution at every step of the procedure," said Chris Landon, Senior Vice President and General Manager Image Guided Therapy Devices, Philips. "Physicians can confidently use a functional guidance strategy across all their patients, including in complex and multi-vessel cases. Today's announcement demonstrates how our unique portfolio of systems, smart devices, software and services combines to deliver advanced procedure-oriented solutions."
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OmniWire is now available in the U.S. and Japan and has received clearance from the U.S. Food and Drug Administration (FDA) and approval from the Japan Pharmaceuticals and Medical Devices Agency.
About Royal Philips
Royal Philips (NYSE: PHG, AEX: PHIA) is a leading health technology company focused on improving people's health and enabling better outcomes across the health continuum from healthy living and prevention, to diagnosis, treatment and home care. Philips leverages advanced technology and deep clinical and consumer insights to deliver integrated solutions. Headquartered in the Netherlands, the company is a leader in diagnostic imaging, image-guided therapy, patient monitoring and health informatics, as well as in consumer health and home care. Philips generated 2019 sales of EUR 19.5 billion and employs approximately 81,000 employees with sales and services in more than 100 countries.
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