In this in-depth profile, 24×7 Magazine spotlights Jovito “Jojo” Gonzales, the 2019 recipient of the AAMI & GE Healthcare “BMET of the Year Award.” Learn how Gonzales got his start in the HTM sector and what advice he would give those entering the profession.
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The U.S. FDA has recalled certain Medtronic MiniMed insulin pumps due to potential cybersecurity risks and recommends that patients using these devices switch their insulin pump to models that are better equipped to protect against these potential risks.
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The FDA is taking steps to update its Medical Device Reporting (MDR) Program, one of the tools the agency uses to monitor device performance, detect potential device-related safety concerns or signals, and contribute to the benefit-risk assessment of these products.
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Cybersecurity provider CSPi and Seceon have linked up to develop a product to address one of the biggest security challenges related to the Internet of Things (IoT): where endpoint detection and response applications and other bolt-on security services cannot be deployed on IoT devices.
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After months of debate regarding the difference between medical device servicing and remanufacturing, the U.S. FDA is planning to publish a draft guidance document on the subject by September 30, an official for the agency revealed during AAMI Exchange 2019.
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