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40 Cards in this Set

  • Front
  • Back
A method of stock rotation that ensures that older items are used first.
First in, first out (FIFO)
Minimum amount of time that packaging materials should be held at room temperature and at 35%-70% relative humidity before sterilization
2 hours
Flat wrapping technique that applies one wrap on top of another to create a package within a package
Sequential
Government agency that regulates sterilization packaging materials
Food and Drug Administration (FDA)
This type of packaging contains no cellulosic materials and would be used to package small items for low temperature sterilization.
Spunbond Polyolefin-Plastic Combinations
This type of packaging can be used in dry heat sterilization but is not recommended for other types of sterilization.
Aluminum Foil
When using paper/plastic pouches, package content information should be written on this side of the pouch
Plastic
True or False: Paperclips are acceptable method of package closure
False
Muslin is an example of this type of packaging material
Reusable
Maximum density recommended per cubic foot of a linen pack
7.2 Pounds
True or False: Sterilization documentation is not required for items that are flash sterilized
False
True or False: Instruments must be cleaned before flash sterilization
True
True or False: Flash sterilization is rarely performed in hospitals
False
True or False: Peracetic acid is a liquid oxidizing agent that effectively kills bacteria at low temperatures
True
True or False: Currently there are no process monitors for peracetic acid sterilization processes
False
True or False: a diagnostic cycle on the peracetic acid system should be run every day
True
True or False: hydrogen peroxide in an example of oxidative chemistry
True
True or False: Liquid peracetic acid is difficult to rinse from items
False
True or False: Ethylene oxide is not used for point of use processing because of its long cycle times
True
True or False: High level disinfection is appropriate for semi-critical devices
True
The procedure used by healthcare facilities to confirm that sterilization recommendations from the manufacturer can be successfully undertaken in the hospital setting is called_____.
Verification
The test used to evaluate the efficacy of a steam sterilizer's air removal system is call a _____ test.
Bowie-Dick
A dating system that records the date as the number of days that have elapsed since January 1st is called the _______.
Julian Date
The ______ is the portion of the steam sterilizer that measures steam temperature and automatically controls the flow of air and condensate from the sterilizer chamber
Thermostatic Trap
Central Service Technicians should never use _______ to hold instruments together for sterilization
Rubber Bands
Steam sterilization heats items within the load using a heat transfer process called ______.
Convection
______ steam sterilization can be used to sterilize liquids
Gravity
The weight of wrapped basin sets should not exceed ______.
7 Pounds
The bacterial spore used for testing dry heat sterilization is __________.
Bacillus atrophaeus
Dry heat sterilization heats items within the load using a heat transfer process called ______.
Conduction
The "newest" low temperature sterilization process
Ozone
This method of low temperature sterilization has been in use since the 1960's
Ethylene Oxide
Cycle time for items sterilized using hydrogen peroxide gas plasma
Less than one hour
Bacterial spore used to test ethylene oxide sterilization cycles
Bacillus atrophaeus
Cycle time for items using ozone sterilization
4 hours
140 degrees F. aeration time recommended for items sterilized with ethylene oxide
8 hours
Bacterial spore used to text hydrogen peroxide gas plasma sterilization cycles
Geobacillus stearothermophilus
Cycle time for items sterilized using using ethylene oxide sterilization
12+ hours
Sets exposure standards for chemical sterilants
OSHA
Requires that sterilants be rigorously tested before being marketed.
FDA