Medical Device and Diagnostic industry
WEBSep 12, 2024. |. 9 Min Read. View More. 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. Register Now.
Recent Industry Events | Medical Device and Diagnostic Industry
WEBMD&M East. Jun 10, 2025 TO Jun 12, 2025. Jacob Javits Convention Center | New York, NY. Medtech moves fast. Keep the pace with the latest innovations and immerse yourself in a community of visionaries and industry leaders. It’s all waiting at the region’s most comprehensive medical design and manufacturing event — MD&M East.
The Top Medical Device Companies of 2023 - MDDI Online
WEBFeb 29, 2024 · Medtronic's Touch Surgery Enterprise allows surgeons to seamlessly and securely upload, store, analyze, and share surgical videos.
Top 100 Medical Device Companies - MDDI Online
WEBJan 25, 2021 · The Top 15 Cardiology companies’ sales in 2019 and 2018. The Top 15 Orthopedic companies’ sales in 2019 and 2018. The Top 15 Imaging companies’ sales in 2019 and 2018. Commentaries on 2019 sales and on 2020-21 and beyond are also available from Medtech Insight and In Vivo: * Medtech Insight’s MTI 100 ranking contains slightly different ...
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. For an overview on other tests in the IEC 60601-1 standard ...
FDA's New MDR Regulations:What Manufacturers Need to Know
WEBOct 1, 1996 · As discussed below, FDA has stayed the new regulations implementing the certification requirement. Section 519 (d) of the FD&C Act expressly authorizes FDA to require manufacturers to certify to the number of MDR reports submitted, and no more. In mandating that manufacturers certify that all reportable events were submitted, FDA exceeded the ...
About MD+DI - MDDI Online
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.
FDA's New MDR Regulations:What Manufacturers Need to Know
WEBOct 1, 1996 · The new regulations require manufacturers to file MDR reports for the same categories of events required under the old regulations: deaths, serious injuries, and certain malfunctions. However, changes in definitions of these terms and in the standard for reporting these categories of events necessitate changes in the analysis used by ...
The Top 10 Cardio Device Companies: Highlights from TCT - MDDI …
WEBOct 12, 2015 · 1. Medtronic. Even after Medtronic's $48 billion merger with Covidien early this year, cardiovascular technology remains the dominant product area for the company, comprising 46% of sales in Medtronic's most recent fiscal year. Before the merger, more than half of the company's revenue came from its cardiovascular segment. Covidien itself brought a $1.2 billion-a-year cardiology business to ...
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 ...