Philips Introduces 160 cm LumiGuide Endovascular Navigation Wire
Philips has introduced a 160cm FDA-approved version of its LumiGuide navigation wire, powered by FORS technology.
Philips has introduced a 160cm FDA-approved version of its LumiGuide navigation wire, powered by FORS technology.
Philips has nabbed U.S. FDA clearance for its X11-4t Mini 3D TEE transducer, designed to provide highly detailed images of the heart for a wider range of patients, including pediatric and complex cases, improving cardiac care and reducing the need for invasive procedures.
The FDA updated a safety communication regarding medical device reports associated with the breakdown of materials used in Philips devices.
Philips has introduced a 160cm FDA-approved version of its LumiGuide navigation wire, powered by FORS technology.
The FDA granted De Novo Clearance for the Philips Inferior Vena Cava Filter Removal Laser Sheath to remove an IVC filter when other methods have failed.
Read MoreInitially cleared for Emergency Use Authorization in 2020, Philips’ MX750 and MX850 patient monitors are designed to support scalability, alarm management, cybersecurity, and enhanced infection prevention within the hospital.
Read MoreRoyal Philips has inked a deal to acquire Cardiologs, a Paris-based medical technology company focused on cardiac diagnostics using artificial intelligence and cloud technology.
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