On May 21, 2020, the U.S. Food and Drug Administration (FDA) issued a guidance to help foster continued availability of medical devices during the COVID-19 public health emergency. Per the g... Read more
U.S. PIRG delivered a letter to congressional lawmakers on Monday, signed by 326 hospital repair experts, calling for manufacturers to stop withholding what technicians need to fix medical e... Read more
FIME Marketing Manager Christina Sanchez sent an email today informing interested parties that FIME 2020 is postponed. “Over the past few months, we have continued to monitor the impact of C... Read more
The U.S. Food and Drug Administration (FDA) is concerned that certain filtering facepiece respirators (respirators) manufactured in China may not provide consistent and adequate respiratory... Read more
The U.S. Food and Drug Administration today announced the following actions taken in its ongoing response effort to the COVID-19 pandemic: The FDA issued an Emergency Use Authorization (EUA)... Read more
The U.S. Food and Drug Administration (FDA) issued the immediately in effect guidance Notifying CDRH of a Permanent Discontinuance or Interruption in Manufacturing of a Device Under Section... Read more
As companies around the world experience shortages of protective gear due to COVID-19, they shift to homemade supplies or use supplies multiple times to make up for the lack of resources. En... Read more
As part of the medical technology industry’s multi-front battle to combat the coronavirus (COVID-19) pandemic, the Advanced Medical Technology Association (AdvaMed) announced the launch of a... Read more
Husco, a privately-held company specializing in high performance hydraulic and electro-mechanical components, today announced that a consortium called MaskForce has designed, developed, and... Read more
The U.S. Food and Drug Administration included, under the ventilator emergency use authorization (EUA), a ventilator developed by the National Aeronautics and Space Administration (NASA), wh... Read more
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