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BMET101 A CABT PREP COURSE QUESTIONS AND CORRECT ANSWERS 100% VERIFIED 2026 UPDATE!!

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BMET101 A CABT PREP COURSE QUESTIONS AND CORRECT ANSWERS 100% VERIFIED 2026 UPDATE!!

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BMET101 A CABT PREP COURSE QUESTIONS AND CORRECT
ANSWERS 100% VERIFIED 2026 UPDATE!!! ALREADY GRADED A+
LATEST UPDATE!!!



Dress Code - (ANSWER)Business Casual Attire or Scrubs/Uniforms



Is it a requirement for BMET's to continue training throughout their career? T/F - (ANSWER)True



Definition of OEM/FSE - (ANSWER)Original Equipment Manufacturer/Field Service Engineer



BMET Core responsibilities - (ANSWER)Repair and Maintenance of Medical Equipment



Define HIPAA - (ANSWER)Health Insurance Portability and Accountability Act



Define MEMP - (ANSWER)Medical Equipment Maintenance Plan



Device Classes (As defined by the FAA) - (ANSWER)Class I devices are low-risk devices. Examples include
bandages, handheld surgical instruments, and nonelectric wheelchairs.



Class II devices are intermediate-risk devices. Examples include computed tomography (CT) scanners or
infusion pumps for intravenous medications.



Class III devices are high-risk devices that are very important to health or sustaining life. Examples
include pacemakers and deep-brain stimulators.



define two levels of recall - (ANSWER)Correction - Addresses a problem with a medical device in the
place where it is used or sold.

Removal - Addresses a problem with a medical device by removing it from where it is used or sold.



Define the Three Classes of Recalls - (ANSWER)Class I: Recalls for products which could cause serious
injury or death;

,BMET101 A CABT PREP COURSE QUESTIONS AND CORRECT
ANSWERS 100% VERIFIED 2026 UPDATE!!! ALREADY GRADED A+
LATEST UPDATE!!!



Class II: Recalls for products which might cause serious injury or temporary illness;



Class III: Recalls for products which are unlikely to cause injury or illness, but that violate FDA
regulations.



What is the SDMA and how is it used? - (ANSWER)Safe Medical Device Act (SMDA) of 1990



Sequester the device and all accessories to ensure the device is not used on another patient

Ensure the device is clearly labeled, "Do Not Use" to ensure another employee in your department does
not put it back into service

Report the incident your supervisor immediately

Document the incident



What is a visual inspection that a HTM performs? - (ANSWER)A visual inspection is a type of inspection
of medical equipment using vision, hearing, touch, and/or smell. Visually inspect a medical device to see
if the equipment is undamaged, plugged-in, and working.



What is a safety check that a HTM performs? - (ANSWER)A safety check on a device is a common test to
ensure the unit is properly grounded and will not cause a shock hazard to the patient or the user. There
is a specific piece of test equipment (seen later in the module) that measures ground resistance and
chassis leakage. Once the unit passes this test then operational and function tests can be performed.



What is a operational check that a HTM performs? - (ANSWER)An operational check is an "out of the
box" examination to ensure the device is not externally damaged and has all of the accessories. The unit
is then set up to be functionally tested.



What is a functional check that a HTM performs? - (ANSWER)A functional check is performed once the
electrical safety check (if applicable) and operational checks are completed. Following the
manufacturer's specifications or recommendations, the functions of the device are tested and verified to
be functioning to be used on a patient or in a lab.

, BMET101 A CABT PREP COURSE QUESTIONS AND CORRECT
ANSWERS 100% VERIFIED 2026 UPDATE!!! ALREADY GRADED A+
LATEST UPDATE!!!




Planned/Preventative Maintenance (PM) - (ANSWER)Planned/Preventative Maintenance (PM) are
scheduled maintenance activities that occur at a defined frequency (e.g.: annually).



high-risk medical equipment - (ANSWER)High-risk medical equipment includes life-support equipment
and would typically require vigorous maintenance



Non-high-risk equipment - (ANSWER)Non-high-risk equipment are the devices not included in the high-
risk category. In other words, there are two categories: high-risk and everything else. Non-high-risk may
or may not require maintenance depending on the device and hospital experience.



Alternative Equipment Maintenance - (ANSWER)An Alternative Equipment Maintenance is any
maintenance procedure that deviates from the manufacturer's recommendations for process or
frequency. To execute an AEM, regulatory agencies require that a formal AEM Plan be documented
showing that the HTM Department evaluated the risks involved and the maintenance history of the
device.



What equipment can and cannot be included in an AEM implementation? Organizations cannot deviate
from these categories of equipment: - (ANSWER)Any imaging device (x-rays, etc.), Lasers, Anything
regulated by state or federal regulations, and

Devices that are new to the industry, as organizations need relative history in order to deviate



Should a hospital follow it's own AEM? - (ANSWER)The hospital or organization must follow its own AEM
program as it is written to be successful.



What service documents would you need to perform an OEM PM? - (ANSWER)Performing OEM (original
equipment manufacturers) preventive maintenance refers to following the manufacturer's
recommended intervals and activities found in the service documentation or service manual. Companies
are not required to provide the service manual but one could be requested or purchased. Calling
technical support is also an option to acquire service information to perform the PM.

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