Iahcsmm chapter 5 Word Scramble
|
Embed Code - If you would like this activity on your web page, copy the script below and paste it into your web page.
Normal Size Small Size show me how
Normal Size Small Size show me how
| Question | Answer |
| agency which may intervene in a matter of worker protection even if there is no specific regulations covering the situation | Occupational Safety and Health Administration (OSHA) |
| regulations under the Clean Air Act are administered by the | Environmental Protection Agency (EPA) |
| agency which imposes very strict labeling requirements on manufacturers of disinfectants used by central service departments | Environmental Protection Agency (EPA) |
| healthcare regulations and standards establish | minimal levels of quality and safety |
| chemical indicators are classified as | FDA Class II medical devices |
| heart valves and pacemakers are examples of | FDA Class IIIfalse medical devices |
| under current regulations, who is required to report suspected medica device-related deaths to the FDA | all of the above |
| standards and regulations help set levels of | quality,safety and efficiency |
| medical device reporting is regulated by | FDA |
| the department of transportation enforce statutes relating to the | transportation of clean and soiled instruments between facilites |
| sometimes state or local regulations differ from federal regulations. when that happens the most stringent regulations apply | true |
| it is optional to follow OSHA regulation for wearing PPE in decomtam. | false |
| third party reprocessors are regulated by the FDA | true |
| recommendations regarding sterilization practices are provided by the association for the advancement of medical instruments (AAMI) | true |
| OSHA is a voluntary association dedicated to infection control and prevention | false |
| failure to receive accreditation from the joint commission can result in the loss of Medicare/Medicaid payments | true |
| the society of gastroenterology nurses and associates is a source of information about the proper processing of flexible endoscopes | true |
| class III medical devices are identified as high risk | true |
| reuse of single use medical devices is less regulated than it was in the 1990's | false |
| the FDA recalls may be either mandatory or voluntary | true |
Created by:
clmcnees