Monash University scientists have developed a new (preclinical) method to distinguish between chronic pain subtypes, such as ...
Significantly more patients with acute migraine who received a 10 L per minute dose of a transnasal cooling device had pain freedom at 2 hours vs. those who received sham, according to research ...
Bengaluru: The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", following reports of the deaths of four patients.
Medtronic has issued a recall for several aortic root cannula devices due to a potential safety risk that could cause loose ...
Medtronic has recalled embolization devices collectively linked to reports of 17 injuries and four deaths, the Food and Drug Administration said Tuesday. The recall has two elements: Medtronic is ...
March 18 (Reuters) - The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's (MDT.N), opens new tab embolization device as "most serious", following reports of the ...
Major companies in the post-operative pain management sector are focusing on technological advancements such as the development of cryoablation probes. These devices target nerves with controlled ...
FDA Classifies Recall of Medtronic Embolization Devices as 'Most Serious' (Reuters) -The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as ...
TriCare, the federal health insurer for the military, has temporarily stopped paying the medical claims of pain management device maker Zynex Medical. In a recent filing with the Securities and ...
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GlobalData on MSNFDA tags Medtronic embolisation device recall as Class IThe US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as ...
The results suggest that nature-based therapies can be used as promising complementary approaches to pain management. In a new study, an international team of neuroscientists led by the University ...
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