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Dear Subscriber,
SunTech Medical has been hard at work testing and preparing our latest product and we are proud to announce the new Tango M2! If you follow our website and blog, you may have already seen some information. If not, we invite you to visit both to learn more.
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SunTech Launches New Tango M2 Automated Cardiac Stress BP Monitor
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 Apr. 1, 2013 - SunTech Medical has updated its line of automated blood pressure monitoring with the Tango® M2 cardiac stress BP monitor. The new product provides accurate BP measurements during exercise and cardiac stress testing where noise and motion often make manual measurements difficult..
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Connectathon 2013: SunTech Medical Passes Testing
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 Feb. 12,2013 - SunTech Medical has successfully passed multiple interoperability tests during 2013 IHE North American Connectathon (Chicago, Ill.)-part of the company's strategy to develop medical products that can easily share data with different electronic healthcare management (EMR) systems.
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8 New 3rd Edition Regulatory Requirements that Impact Automated Non-invasive Blood Pressure.
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Written by Scott Scargle
If you're a medical device developer or active in the design process, you've probably been involved with creating a list of "must have" and "nice to have" features and requirements for a new or updated medical device. Some come from market feedback, industry trends, competitor analysis, R&D and others come from medical equipment regulatory standards. When it comes to safety and meeting regulatory standards, this is always in the mandatory column. With several deadlines looming on the horizon, meeting the latest 3rd edition standards as well as being RoHS compliant are on almost everyone's must have list when starting a new project. So whether you are developing your own NIBP or purchasing OEM NIBP modules, you now have new requirements that need to be a part of your design not only in hardware and software but also in the product's technical documentation.
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