Medical Device + Diagnostic Industry
WEBRAS Systems, Instruments & Implants Manufacturing. May 22, 2024. |. 11:00 EDT. Medical Device and Diagnostic Industry (MD+DI) is the primary resource for manufacturers of medical devices and in vitro diagnostic products.
The Top Medical Device Companies of 2023 - mddionline.com
WEBFeb 29, 2024 · Medtech in a Minute is a weekly video highlighting the top industry news of the week.
Leakage Current Standards Simplified - mddionline.com
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 …
Brain-Computer Interface Tech Hits a Huge Milestone
WEBJul 19, 2022 · The FDA granted Synchron a breakthrough device designation in August 2020. “The first-in-human implant of an endovascular [brain-computer interface] in the U.S. is a major clinical milestone that opens up new possibilities for patients with paralysis,” said Tom Oxley, MD, PhD, Synchron's CEO and founder. “Our technology is for the ...
Top 100 Medical Device Companies - mddionline.com
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 …
Medtronic Hit with Recall over Recently Approved Varicose Vein …
WEBMay 18, 2015 · Medtronic (Dublin, Ireland) sent out a recall notification via letter and email on April 28. Mansfield, MA was listed as the manufacturer's address. The technology was actually developed by Sapheon Inc. (Morrisville, NC), which Covidien acquired last year. Medtronic then acquired Covidien in a $48 billion deal that closed in January.
FDA Updates Guidance on Reprocessing of Single-Use Devices
WEBOct 1, 2006 · FDA's revised guidance comes at a time when certain states have passed or are considering laws regarding the use of reprocessed SUDs. A Utah law “requires a reprocessor of a critical single-use medical device to assume the liability associated with the original manufacturing and the reprocessing of the critical single-use medical device.”.
Medtronic Takes DES to a New Frontier - mddionline.com
WEBAug 24, 2022 · The Onyx Frontier DES is used for the treatment of patients with coronary artery disease (CAD), which is caused by plaque buildup on the inside of the coronary arteries. These plaque deposits can narrow or clog the inside of the arteries, which decreases the supply of blood and oxygen to the heart. To help to restore blood flow, a …
Teladoc Acquires Livongo as Demand for Virtual Care Swells
WEBAug 5, 2020 · natali_mis -stock.adobe.com. Teladoc Health is acquiring Livongo in a deal valued at $18.5 billion as the pandemic is causing demand for virtual care to be at an all-time high. The transaction has been unanimously approved by the boards of each company. Each share of Livongo will be exchanged for 0.5920x shares of Teladoc Health plus cash ...
Indiana’s Medical Device Mecca Has Good Bones
WEBNov 9, 2008 · The secret to Northern Indiana's success is easy to decipher, concludes Emerick: In the 1890s, DePuy started his company. In the 1920s, Zimmer left DePuy and started his own company. In the 1970s, Dane Miller left Zimmer and started Biomet. The presence of the Big 3 automatically gave rise to dozens of suppliers around them.
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