2.Which of the following statement(s) is(are) true? (a) Both static and dynamic
ID: 2085159 • Letter: 2
Question
2.Which of the following statement(s) is(are) true?
(a) Both static and dynamic LIM provides only indication of issues, and therefore
they do not provide the necessary power protection to the patients.
(b) Pull stations, as well as sprinkler systems, should be checked once
every 12 months.
(c) Electrical shocks are the primary occupational hazard for biomedical technicians
(d) Every hospital and medical facility has policies and procedures that address
infectious materials and additional measures that can be taken to prevent the
spread of diseases and it is the employees's responsibilities to get educated on
these policies and procedures.
(e) Safety Medical Device Acts requires manufacturers report adverse events
Explanation / Answer
(a) False. Both 3rd generation static and dynamic LIM provides only indication of issues, and therefore
they do provide the necessary power protection to the patients. it must be remembered that the LIM not designed to protection from microshocks. the microampere current involved in micorshocks are far below than LIM threshold of protection.
(b) False. pull station and Sprinkler has to be changed when they are used. if not 90 days checking is neccesary.
(c) false.
(d). True. Infection management addresses factors associated with the unfold of infections at intervals the care setting (whether patient-to-patient, from patients to employees and from employees to patients, or among-staff), as well as hindrance (via hand hygiene/hand laundry, cleaning/disinfection/sterilization, vaccination, surveillance), monitoring/investigation of incontestible or suspected unfold of infection at intervals a specific health-care setting (surveillance and occurrenceinvestigation), and management (interruption of outbreaks). it's on this basis that the common title being adopted at intervals health care is "infection hindrance and management."
(e) True. Manufacturers square measure needed to report back to the office once they learn that any of their devices could have caused or contributed to a death or serious injury. (Key terms square measure outlined in twenty one CFR 803.3.) directions square measure on the market for finishing the desired 3500A kind. makers should additionally report back to the office once they become aware that their device has malfunctioned and would be possible to cause or contribute to a death or serious injury if the malfunction were to recur. For a lot of info please see the steerage for makerson medical device coverage.
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