The U.S. Food and Drug Administration announced the following actions taken in its ongoing response effort to the COVID-19 pandemic: The FDA issued an updated FDA COVID-19 Response At... Read more
COVID-19 hot spots across the nation are receiving 6,000 3D-printed face shields to protect the healthcare technology management (HTM) professionals responsible for managing and maintaining... Read more
Royal Philips has announced that the U.S. FDA has issued an Emergency Use Authorization (EUA) for Philips’ IntelliVue Patient Monitors MX750/MX850 and its IntelliVue Active Displays A... Read more
The U.S. Food and Drug Administration today continued to take action in the ongoing response to the COVID-19 pandemic: The FDA issued an Emergency Use Authorization for the Stryker Su... 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
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
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