COVID-19 did its fair share of damage, but it also forced the adoption of telehealth technologies and remote patient monitoring within healthcare facilities so patients could contact their doctors fro...Read More
As many are aware, COVID-19 has negatively affected most businesses, industries, and markets. However, the demand for patient monitoring equipment in Europe saw it differently. Patient monitoring devi...Read More
Vitls Inc., a company based out of Houston, Texas, has received 510(k) clearance from the FDA for its Vitls Platform, a telemonitoring system. This platform provides a streamlined process of vital sig...Read More
Bardy Diagnostics‘ 14-day Carnation Ambulatory Monitor (CAM) patches have previously been used in U.S. hospital settings, but they have now been granted a CE mark for these products. The patches...Read More
The FDA has recently granted clearance for the portable AiRTouch X-ray device developed by Aspenstate to be used for humans. This small, handheld device joins the array of telehealth products being de...Read More
The FDA has recently granted 510(k) clearance to Philips for a range of its devices to be used to manage COVID-19 patients in the U.S. The approved products include the Affiniti series, EPIQ series, L...Read More
In Europe, respiratory device manufacturer ResMed has accelerated their process of launching remote tracking of ventilators, to combat the ongoing COVID-19 crisis. This cloud-based technology provides...Read More
Register to receive a free US Patient Monitoring Market Report Suite 2019-2025 synopsis and brochure The telemedicine market has grown tremendously in recent years, powered by increasing awareness o...Read More
Register to receive a free US Patient Monitoring Market Report Suite 2017-2023 synopsis and brochure Telemedicine research released by iData Research demonstrates that the national telehealth market v...Read More