CBSPD Practice Exam 1 State Certification Endoscope
2023 with complete solution
Which of the following agencies regulates clearances for glutaraldehyde-based
disinfectants?
- OSHA
- CDC
- EPA
- FDA
FDA
Which agency is responsible for employee health and safety at work?
- EPA
- FDA
- CDC
- OSHA
OSHA
Recommended practices are:
- Statements of sound principles of practice that are based on scientific data and the
opinions of experts
- Principles, laws, or rules designed to govern behavior
- Documents that reflects state and federal regulations
- Established norms determined by opinion, authority, research, and/or theory
Statements of sound principals of practice that are based on scientific data and the
opinions of experts.
Which of the following agencies registers and regulates environmental disinfectants
used on
non-living things in healthcare facilities?
- EPA
- NFPA
- OSHA
- FDA
EPA
Reprocessing of single-use devices is regulated by the :
- OSHA
- FDA
- TJC
- CDC
FDA
Which of the following has published standards of infection prevention in processing
flexible
gastrointestinal endoscopes?
- EPA
- FDA
- AAMI
- SGNA
, SGNA
Which of the following must be provided by the chemical manufacturer for every
the chemical used in the department?
- Approval notice from Infection Control
- Product distributer
- Safety Data Sheets (SDS)
- Facility contract
Safety data sheets (SDS)
According to Earl Spaulding, devices that come in contact with intact mucous
membranes during use are classified as :
- Sterile
- Semicritical
- Critical
- Noncritical
Semicritical
The policies and procedures for all reprocessing activities in the GI/endoscopy suite are
usually reviewed and/or approved by the :
- Supervisors and managers
- staff performing the reprocessing
- physicians performing the procedures
- Infection Prevention and Control Committiee
Infection Prevention and Control Committee
Which agency requires medical device manufacturers to provide end-users in
healthcare
facilities with specific instructions on how to reprocess their reusable products?
- FDA
- CDC
- OSHA
- AAMI
FDA
Environmental disinfectants should never bu used on :
- Items that contact the patient
- Patient beds
- Medical equipment
- Tables in the processing room
Items that contact the patient
Compliance with OSHA regulations is :
- Optional
- Required by law
- Only required during unsafe practices
- Recommended whenever there is time
Required by law
According to Spaulding's classification of medical devices, a semicritical item requires
which of the following?
- High-level disinfection
- Sanitization
2023 with complete solution
Which of the following agencies regulates clearances for glutaraldehyde-based
disinfectants?
- OSHA
- CDC
- EPA
- FDA
FDA
Which agency is responsible for employee health and safety at work?
- EPA
- FDA
- CDC
- OSHA
OSHA
Recommended practices are:
- Statements of sound principles of practice that are based on scientific data and the
opinions of experts
- Principles, laws, or rules designed to govern behavior
- Documents that reflects state and federal regulations
- Established norms determined by opinion, authority, research, and/or theory
Statements of sound principals of practice that are based on scientific data and the
opinions of experts.
Which of the following agencies registers and regulates environmental disinfectants
used on
non-living things in healthcare facilities?
- EPA
- NFPA
- OSHA
- FDA
EPA
Reprocessing of single-use devices is regulated by the :
- OSHA
- FDA
- TJC
- CDC
FDA
Which of the following has published standards of infection prevention in processing
flexible
gastrointestinal endoscopes?
- EPA
- FDA
- AAMI
- SGNA
, SGNA
Which of the following must be provided by the chemical manufacturer for every
the chemical used in the department?
- Approval notice from Infection Control
- Product distributer
- Safety Data Sheets (SDS)
- Facility contract
Safety data sheets (SDS)
According to Earl Spaulding, devices that come in contact with intact mucous
membranes during use are classified as :
- Sterile
- Semicritical
- Critical
- Noncritical
Semicritical
The policies and procedures for all reprocessing activities in the GI/endoscopy suite are
usually reviewed and/or approved by the :
- Supervisors and managers
- staff performing the reprocessing
- physicians performing the procedures
- Infection Prevention and Control Committiee
Infection Prevention and Control Committee
Which agency requires medical device manufacturers to provide end-users in
healthcare
facilities with specific instructions on how to reprocess their reusable products?
- FDA
- CDC
- OSHA
- AAMI
FDA
Environmental disinfectants should never bu used on :
- Items that contact the patient
- Patient beds
- Medical equipment
- Tables in the processing room
Items that contact the patient
Compliance with OSHA regulations is :
- Optional
- Required by law
- Only required during unsafe practices
- Recommended whenever there is time
Required by law
According to Spaulding's classification of medical devices, a semicritical item requires
which of the following?
- High-level disinfection
- Sanitization
