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A Checklist For Purchasing New Surgical Instruments Part III

The first step in reducing patients’ risk of a surgical site infection (SSI) caused by a contaminated surgical instrument begins with an in-depth assessment of the various brands and options that are available prior to making the final purchasing decision. According to the Association for the Advancement of Medical Instrumentation...

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News

“A Checklist For Purchasing New Surgical Instruments Part II”

The first step in reducing your patients’ risk of a surgical site infection (SSI) caused by a contaminated surgical instrument begins with an in-depth assessment of the various brands and options that are available prior to making the final purchasing decision. According to the Association for the Advancement of Medical...

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News

FDA’s Validated IFU Requirements For “High Risk” Devices (Part II)

In Part I of this blog (Novo blog number 115, 12/13/19) we pointed out that “The #1 responsibility of everyone involved in reusable medical device processing is to minimize the risk of patient harm caused by a device that remains contaminated with organic debris after processing.” The responsibility to minimize...

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News

FDA’s Validated IFU Requirements For “High Risk” Devices (Part I)

The #1 responsibility of everyone involved in reusable medical device processing is to minimize the risk of patient harm caused by a device that remains contaminated with organic debris after processing. This responsibility begins with pre-cleaning the device at point of use and it continues through all of the processing...

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