SP 107: Medical Device Cleaning Decisions
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This presentation will look at how standards, IFUs, FDA guidance, and facility policy translate into practical medical device cleaning decisions. It will highlight the key variables and evidence used to determine whether a device can proceed to the next processing step or requires additional action.
Key:
Kaumudi Kulkarni
Program Manager, Sales & Service Support
Healthmark, A Getinge company
Kaumudi Kulkarni is the Senior Manager of Research and Development at Healthmark Ind. Kaumudi has been part of the medical device reprocessing industry for more than 10 years and has spent her career working with medical device manufacturers, sterile processing professionals and independent testing laboratories along with the other professional groups and organizations. With her expertise, Healthmark is better able to help meet the ever changing regulatory environment for instrument reprocessing. A voting member at AAMI and ASTM, Kaumudi is also actively involved in developing products that help improve patient care outcomes.