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Items 101 ~ 120 of 2699, Page 6 of 136
101. Medtronic Announces Worldwide Voluntary Field Corrective Action; Company Issues Software Update for Puritan Bennett(TM) 980 (PB980) Ventilator Series
Medtronic (NYSE:MDT) is notifying customers worldwide of a voluntary field corrective action for its Puritan Bennett(TM) 980 (PB980) ventilator series.?Medtronic initiated this field action on September 19, 2018.
12/04/2018 Medtronic
102. Medtronic Announces First Patient Treated in TERMINATE AF Clinical Trial
Study Will Evaluate Simultaneous Use of Radiofrequency and Cryo Surgical Ablation Devices in Cardiac Surgery Patients with Atrial Fibrillation
12/03/2018 Medtronic
103. FDA approves first biosimilar for treatment of adult patients with non-Hodgkin’s lymphoma
The agency has now approved 15 biosimilars and is advancing new policies to improve the efficiency of biosimilar development and review
104. Cryoablation Shows Promise in Treating Low-Risk Breast Cancers
Cryoablation may offer a promising alternative for treating early, low-risk breast cancers.
11/28/2018 Radiological Society of North America
105. Statement from FDA Commissioner Scott Gottlieb, M.D., on how modern predicates can promote innovation and advance safety and effectiveness of medical devices that use 510(k) pathway
106. Pulsed Radiofrequency Relieves Acute Back Pain and Sciatica
Pulsed energy to treat acute lower back pain is safe and effective.
11/27/2018 Radiological Society of North America
107. Statement from FDA Commissioner Scott Gottlieb, M.D. and Jeff Shuren, M.D., Director of the Center for Devices and Radiological Health, on transformative new steps to modernize FDA’s 510(k) program to advance the review of the safety and effectiveness of medical devices
Modernizing the 510(k) Pathway“Safety and Performance Based Pathway” / Promoting Greater Transparency and Post-Market Surveillance
108. Artificial Intelligence Research Receives RSNA Margulis Award
The Radiological Society of North America (RSNA) presented its seventh Alexander R. Margulis Award for Scientific Excellence to Paras Lakhani, M.D., from Thomas Jefferson University Hospital (TJUH) in Philadelphia, for the article, Deep Learning at Chest Radiography: Automated Classification of Pulmonary Tuberculosis by Using Convolutional Neural Networks, ...
11/26/2018 Radiological Society of North America
109. Artificial Intelligence May Help Reduce Gadolinium Dose in MRI
A deep learning algorithm may allow for gadolinium dose reduction in MRI exams.
11/26/2018 Radiological Society of North America
110. RSNA Recognizes Winners of Pneumonia Detection Machine Learning Challenge
The RSNA Pneumonia Detection Challenge required teams to develop algorithms to identify and localize pneumonia in chest X-rays. Over 1,400 teams took part in the challenge, and 346 submitted results during the evaluation phase of the competition.
11/26/2018 Radiological Society of North America
111. Abbott Initiates Study to Evaluate Ablation as a Frontline Treatment for Patient''s Suffering from a Common but Complex Cardiac Arrhythmia
LESS-VT Study is the first U.S. clinical trial to evaluate the safety and effectiveness of ablation treatment for patients with monomorphic ventricular tachycardia, a common heart rhythm disorder
11/20/2018 Abbott
112. Statement from FDA Commissioner Scott Gottlieb, M.D. and Jeff Shuren, M.D., Director of the Center for Devices and Radiological Health, on FDA’s updates to Medical Device Safety Action Plan to enhance post-market safety
113. CDC Establishes AFM Task Force
CDC Director Robert R. Redfield, M.D., announced today the establishment of an Acute Flaccid Myelitis (AFM) Task Force (Task Force) to aid in the ongoing investigation to define the cause of, and improve treatment and outcomes for, patients with AFM.
11/19/2018 Centers for Disease Control and Prevention
114. Statement by FDA Commissioner Scott Gottlieb, M.D., on the FDA’s efforts to hold industry accountable for fulfilling critical post-marketing studies of the benefits, safety of new drugs
115. Statement from USDA Secretary Perdue and FDA Commissioner Gottlieb on the regulation of cell-cultured food products from cell lines of livestock and poultry
116. New Findings Presented at the VEITHsymposium Reiterate Consistent, Durable Outcomes in Complex Aortic Disease with Heli-FX(TM) Endoanchor(TM) System
Three-Year Data from the ANCHOR Registry Reiterate Applicability in Patients with Hostile Aortic Neck Anatomies
11/16/2018 Medtronic
117. New Approvals Allow Chronic Pain Sufferers to Try Abbott''s Non-Opioid Pain Therapy Before Getting Device Implant
Neurostimulation of the dorsal root ganglion (DRG) can provide pain relief for patients battling chronic pain when previous treatment options were unsuccessful / Abbott's new DRG Invisible Trial System brings an intuitive, wireless approach to the temporary evaluation giving patients the full benefits of DRG therapy prior to permanent implant
11/15/2018 Abbott
118. Abbott and The Chertoff Group Explore Current State of Cybersecurity in the Connected Hospital
New White Paper Shares Research Findings on Perceptions and Awareness of Medical Device Cybersecurity, Need for Collaboration to Address Cybersecurity Challenges
11/15/2018 Abbott
119. FDA alerts doctors, patients about risk of complications when certain implanted pumps are used to deliver pain medications not approved for use with the devices
120. Merck Begins Rolling Submission of Licensure Application for V920 (rVSV G-ZEBOV-GP) to U.S. Food and Drug Administration
V920 is the Company's Investigational Vaccine for Ebola Zaire
11/13/2018 MERCK
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