Medical Device and Diagnostic industry
WEBDesign & Engineering What Should Engineers Know About User-Centered Design? MEDevice Boston, the essential event for medtech pioneers, brings engineers, business leaders, disruptive companies, and innovative thinkers from the region’s top start-ups and medical device OEMs together to inspire the next life-changing medical device.
The Top Medical Device Companies of 2023 - MDDI Online
WEBFeb 29, 2024 · See which medical device companies have risen to the top of the leaderboard this year. Is your employer on the list?
About MD+DI
WEBAbout. Medical Device and Diagnostic Industry (MD+DI) is the primary resource for manufacturers of medical devices and in vitro diagnostic products. Its mission is to help medtech industry professionals develop, design, and manufacture products that comply with complex and demanding regulations and evolving market requirements.
Medtronic Pacemaker Linked to Rare (but Major) Complication Risk
WEBNov 17, 2021 · Although cardiac perforation is a rare complication (occuring in roughly 1% of cases) of any pacemaker implant procedure, real-world data suggests that the risk of major complications following cardiac perforation may be higher in patients who receive a Medtronic Micra leadless pacing system versus a traditional transvenous pacemaker.
Caldera Medical Completes Acquisition of Atlantic Therapeutics
WEBSep 6, 2023 · Caldera Medical, a women’s health medical device company, today announced the completion of its acquisition of Atlantic Therapeutics, a provider of non-invasive pelvic floor strengthening and nerve stimulation solutions for women. Caldera solely focuses on medical devices for women’s health, manufacturing and marketing surgical products for ...
Leakage Current Standards Simplified - MDDI Online
WEBJul 1, 2004 · The IEC 60601-1 standard, “Medical Electrical Equipment—Part 1: General Requirements for Safety and Essential Performance,” describes tests for leakage current, as do a number of related national standards.1 This article aims to simplify these tests and the requirements of related standards and explain the rationale behind them.
‘Shouting Out’ Support for Medical Device Customers
WEBMay 25, 2021 · Because of this, this probably explains the very low number of printers that have achieved this certification. In fact, most medical device companies find the ISO 9001 certification to be sufficient for their purposes of qualifying vendors. But we really wanted to “shout” our support for our customers in this specific industry, and the ...
FDA Grants Breakthrough Designation to 'Artificial Meniscus'
WEBSep 19, 2019 · The designation allows an expedited review of the NUsurface meniscus implant from Active Implants. The NUsurface meniscus implant is the first “artificial meniscus” to be marketed in Europe and, if cleared by FDA, would be the first artificial meniscus in the United States, according to Active Implants. Courtesy of …
BD and CareFusion Complete $12 Billion Merger - MDDI Online
WEBMar 16, 2015 · The roughly $12 billion merger between Becton, Dickinson and Co. and CareFusion is expected to close Tuesday, March 17, according to the two companies. The news came after the acquisition overcame its final hurdle, clearance from the European Commission under the EU Merger Regulation. CareFusion (San Diego) will operate as part of the Medical ...
The EU MDR: Post Market Clinical Follow-up (PMCF) End User …
WEBJul 7, 2020 · End-user surveys offer a cost-effective approach for assembling evidence for post-market clinical follow-up for EU MDR compliance.