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When companies are testing a medical device’s bioburden – a measure of how much and what types of viable organisms are in or on it after manufacturing – they might question how exact their results should be or what to do if the numbers seem off.
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When companies are testing a medical device’s bioburden – a measure of how much and what types of viable organisms are in or on it after manufacturing – they might question how exact their results should be or what to do if the numbers seem off.
READ MORE
A new standard that establishes the quality of water used to process reusable medical devices heralds “a huge shift for the health care industry,” in the words of Terra Kremer, a microbiological quality expert and co-chair of the AAMI working group that developed the standard.
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While the AAMI eXchange 2022 is an industry event most commonly attended by medical device manufacturers and the hospital technicians who maintain those devices, it features a robust track of sessions dedicated to the sterile processing of devices starting from...
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A new standard that establishes the quality of water used to process reusable medical devices heralds “a huge shift for the health care industry,” in the words of Terra Kremer, a microbiological quality expert and co-chair of the AAMI working group that developed the standard.
READ MORE
AAMI recently announced that the FDA has added 13 guidance documents produced by AAMI or its standards committees to its database of Recognized Consensus Standards. Of the 13, several have special relevance for the operating room or greater health care facility.
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For over 20 years, OR Today has provided perioperative and SPD professionals with up-to-date news and information about their profession. The magazine aims to educate readers about new guidelines, techniques, and equipment, as well as practical information for career building, problem-solving and overall well-being.
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