The policies and procedures in the Medical Device Reprocessing Department should meet the criteria formulated by the CSA (Canadian Standards Association) and stimulate best reprocessing practice as indicated in the "Ministry of Ontario Best Practices PIDAC" document. - ANS true
Medical D...
The policies and procedures in the Medical Device Reprocessing Department should meet the
criteria formulated by the CSA (Canadian Standards Association) and stimulate best
reprocessing practice as indicated in the "Ministry of Ontario Best Practices PIDAC" document. -
ANS true
Medical Device Reprocessing Departments are very active, and a critical area within a
healthcare facility and in most cases are centrally located, and close to the patient care areas.
In order to provide the environment for learning and understanding of the scope of work, these
departments allow various hospital personnel to frequently visit the area. - ANS false
The organizational structure in an MDRD is determined by the principal functions of the unit,task
assignment, and resource allocation. - ANS true
MDRD serves and supports patient care areas. Staff must demonstrate reliability by delivering
supplies of appropriate quality and quantity as quickly as possible when needed. - ANS
true
MDRD personnel must be courteous, willing and knowledgeable at all times. By being so,
personnel in user areas will develop positive and cooperative attitudes toward the MDRD
making the job of all personnel more pleasant. - ANS true
The Decontamination area is a clean area. - ANS false
Flow in MDRD is a one-way flow. - ANS true
Assembly Area: All disassembled devices are inspected, reassembled and tested, checked to
confirm in working order, packaged appropriately and labeled. - ANS true
Sterilizing Area: Where sterilized items are stored to prevent contamination prior to being
transported to the user areas. - ANS false
Storage & Distribution: Where the sterilization process occurs and monitoring of the process. -
ANS false
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