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MEDICAL DEVICE REPROCESSING ASSOCIATION OF ONTARIO THETA CHAPTER 8th EDUCATION DAY April 20th & 21st 2018 www.mdrao.ca LOCATION: North Bay Hotel Information Best Western 700 Lake shore Drive North
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How to fill out medical device reprocessing

01
Gather all necessary equipment and supplies for the reprocessing process.
02
Clean the medical devices thoroughly using an appropriate cleaning solution or detergent.
03
Rinse the devices with clean water to remove any residual cleaning solution.
04
Inspect the devices for any visible damage or contamination.
05
Disinfect the devices using an approved disinfectant solution or method.
06
Rinse the devices again to remove any residual disinfectant.
07
Dry the devices using a clean, lint-free cloth or by air-drying.
08
Package the reprocessed devices appropriately for storage or reuse, following any specific guidelines or regulations.
09
Label the packages with necessary information such as the reprocessing date and the person responsible for the reprocessing.
10
Store the reprocessed devices in a designated area or according to the facility's storage requirements.

Who needs medical device reprocessing?

01
Medical device reprocessing is needed by healthcare facilities, such as hospitals, clinics, and surgical centers.
02
It is also necessary for medical device manufacturers to ensure the reprocessing of their devices meets industry standards and regulations.
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Medical device reprocessing refers to the processes used to clean, disinfect, and sterilize reusable medical devices so that they can be safely used on patients after their initial use.
Manufacturers and facilities that engage in the reprocessing of medical devices are required to file medical device reprocessing documentation.
To fill out medical device reprocessing documentation, one must provide details including the device type, reprocessing method, validation data, and compliance with applicable regulations.
The purpose of medical device reprocessing is to ensure that reusable medical devices are safe for patient use, reduce costs of healthcare, and minimize medical waste.
Information that must be reported includes device identification, reprocessing methods, validation protocols, safety and efficacy data, and records of prior usage.
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