The remote patient monitoring field is a rapidly growing one given the advantages it offers for home healthcare, remote regions, and elderly care. However, with it comes a long list of considerations and critical issues for designers and engineers to keep in mind. This article offers a “bird’s eye view” of this sector and many of the factors on which to maintain focus.
Barbed fittings for use with plastic and rubber tubing and reinforced hose are available from NewAge Industries in five materials. Each material – polypropylene, polyethylene, nylon, PVDF, and brass – offers different performance properties to meet the demands of diverse applications.
Precipart will be exhibiting at MD&M East, June 18 – 20, 2013 in Philadelphia, with a wide range of high-precision machined, molded and assembled components used in medical devices. Precipart will be featuring several examples of its motion control technology along with a variety of mechanical components...
Pawling Engineered Products has launched a new line of inflatable seal compounds that have earned U.S. Pharmacopoeia Class VI certification. The CVI Series is especially designed for inflatable seals used in a wide range of pharmaceutical and medical seal applications.
Industry-wide, companies of all sizes are discovering one of the most effective tools in business growth—collaboration. Gartner Research Group findings cite that collaborative capabilities have allowed top patient care organizations to make great strides in enabling high-quality care at optimal economic cost.
A new investigational device—the Helio System (TF-FA) —being developed for use with the Sapien XT Transcatheter Heart Valve was successfully deployed in all four patients in a small, first-in-human feasibility study of its use in high-risk aortic insufficiency reported at EuroPCR 2013.
Transcatheter aortic valve implantation is effective and safe in Asian patients, according to early experience based on first results from a multicentre Asian registry reported at EuroPCR 2013. "TAVI has become a treatment option for selected patients with symptomatic severe aortic stenosis. But current data are virtually all from North American or European centres," Paul Chiam told the conference.
Nephosity, a digital health startup that was a member of Rock Health’s second class, has received clearance from the United States Food and Drug Administration (FDA) for their MobileCT Viewer, a software application for diagnostic image viewing on the iPad.
In this video, a representative at Nephosity demonstrates MobileCT, an app for mobile collaborative teleradiology. It allows for a user (such as a doctor or patient) to use their mobile devices to view x-rays, MRIs, etc., and to collaborate with other users (such as other doctors or relatives).
Sensus Healthcare is pleased to announce that it has received clearance from the U.S. Food and Drug Administration to treat Keloids with the SRT-100™. The SRT-100™ is the leading alternative to surgery in treating Non Melanoma Skin Cancer and now is approved to treat Keloids caused by surgery or injury.
Professor Brian T. Cunningham and his graduate students demonstrate their development of using a smartphone camera as a high resolution spectrophotometer. Cunningham’s group is now collaborating with other groups across campus at the U. of I. to explore applications for the iPhone biosensor.
Researchers and physicians in the field could soon run on-the-spot tests for environmental toxins, medical diagnostics, food safety and more with their smartphones. University of Illinois at Urbana-Champaign researchers have developed a cradle and app for the iPhone that uses the phone’s built-in camera and processing power as a biosensor to detect toxins, proteins, bacteria, viruses, and other molecules.
PARIS & MENLO PARK, Calif.--(BUSINESS WIRE)--May 24, 2013--CardioKinetix Inc., a medical device company pioneering a catheter-based treatment for heart failure, today announced the transmission of a live satellite feed of a clinical case using the first-of-its-kind catheter-based Parachute ®...
Reason for Recall: Cook Medical received a small number of complaints that the delivery system of the device had separated at the tip of the inner catheter. Potential adverse events that may occur in cases where the inner deliver catheter breakage...
Below are Premarket Approvals (PMA), Product Development Protocols (PDP), Supplement and Notice Decisions. This list is generated on a monthly basis. A PDF document that contains the "Approval letter and Summary of Safety and Effectiveness" is being added to this listing for each PMA. The PMA number will appear as a link if this document is available.