Approval Of Latest Mobile Ultrasound Technology By FDA

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The VISIQ ultrasound system designed by Philips has been given the clearance by the US Food and Drug Administration (FDA) to publicize the ultrasound system for increasing the quality of the scans in order to optimize the diagnosis of OB (or obstetric care) patients. It has a great quality of system for mobility and has a long battery life.

The VISIQ system is highly effective for OB and abdominal applications and is provided with a transducer that fits easily in the user’s hand. It is manufactured in order to devise a highly advanced modality that may serve as a miniature form of sophisticated broadband, micro digital beam former and powerful acquisition module.

A tablet display touch screen is connected to the transducer through which images and measurements can be taken and with a built in WiFi, data can be easily transferred to the hospitals or cloud based PACS. Moreover, it comes with Philips’ EPIQ system that offers automatic image optimization features.

VISIQ is commercially available in China, East Africa, France, Germany and India to help the doctors in performing the diagnostic scan which is quite helpful for patients to avoid visiting different laboratories.

The information above was given by Gene Saragnese, CEO, Imaging System and Philips Healthcare in the release.

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