CSSD Cheat Sheet 2026
The 30 highest-yield CSSD facts, distilled from real exam questions. Print it, save it as a PDF, or study it here — free, no sign-up.
100 questions
180 min time limit
70% to pass
- A dynamic-air-removal steam sterilization cycle, such as a prevacuum cycle, consists of three main phases. What is the correct sequence of these phases? → Conditioning, Exposure, Drying
- Hygrometer is an equipment: → To measure the humidity level
- Which federal agency regulates the registration and use of sterilants and high-level disinfectants as pesticides in US healthcare? → EPA
- What is the full form of SAL? → Sterility Assurance Level
- According to the event-related policy, how many years can you store a sterile item in the sterile storage cabinet? → 3 years
- PH of Acidic solution should be: → 1-5
- Which sterilization method involves using high-pressure steam to kill microorganisms? → Autoclave sterilization
- Which regulatory body publishes guidelines that support instrument tracking practices and event-related sterility in US healthcare facilities? → Association for the Advancement of Medical Instrumentation (AAMI)
- What is the easiest method of sterilization? → Steam sterilization
- Which of the following describes the correct storage practice for a reprocessed flexible endoscope according to AAMI ST91? → Hung vertically in a designated, clean, and well-ventilated cabinet.
- A CSSD is preparing to package a delicate, sharp instrument in a peel pouch for steam sterilization. Which of the following is a critical step in this process? → Using a foam insert or tip protector to prevent the instrument from puncturing the pouch.
- What is the recommended practice when a sterilized instrument set is found with a broken seal or torn wrapper? → Consider the set non-sterile, return it to decontamination, and reprocess it
- What information must be included on a package label according to AAMI ST79 labeling requirements? → Lot control number, sterilizer number, load number, and expiration date or cycle date
- What is the FIRST action CSSD staff should take before reprocessing loaner instruments? → Review and follow the manufacturer's IFU
- The sterilant in an Ozone (O3) sterilization system is created from which commonly available utilities? → Oxygen, water, and electricity
- What information is typically encoded in an instrument tray's barcode label to support lot control? → Sterilizer load number, date, and cycle parameters
- What is the purpose of applying an external chemical indicator (CI) to the outside of a sterile package? → To show that the package was exposed to the sterilization process
- An example of a sterilant is: → All of the above
- What is OSHA's Bloodborne Pathogen Standard (29 CFR 1910.1030) primarily designed to protect CSSD workers from? → Exposure to blood and other potentially infectious materials (OPIM)
- In steam sterilization terminology, what does the D-value represent? → The time required to reduce the microbial population by 90% at a specific temperature.
- What is the primary purpose of maintaining a 'loaner log' in the CSSD? → To track receipt, processing, sterilization, and return of loaner instruments
- What does the FDA 510(k) clearance process require for reprocessed single-use devices (SUDs)? → Demonstrated equivalence to the original device in safety and effectiveness
- After a flexible endoscope undergoes high-level disinfection, what is the required quality for the water used in the final rinse steps? → Sterile or bacteria-free water.
- Which of the following components is NOT typically part of a Bookwalter retractor system? → A handheld, single-piece frame
- The process of cavitation, which uses microscopic bubbles imploding to dislodge soil from instrument surfaces, is characteristic of which cleaning method? → Ultrasonic Cleaner
- What is a 'count sheet' used for in CSSD instrument set management? → Listing every instrument in a tray to verify completeness before and after use
- What is a 'tray audit' in the context of loaner instrument management? → Verification that all items on the inventory sheet are present in the set
- When managing sterile storage, which of the following practices is essential for maintaining the sterility and integrity of supplies? → Limiting access to the sterile storage area to authorized personnel only.
- Which Centers for Disease Control and Prevention (CDC) guidelines address disinfection and sterilization practices in healthcare settings? → CDC Guideline for Disinfection and Sterilization in Healthcare Facilities
- Before accepting a loaner set from a vendor, which verification step is most critical? → Confirming the set arrived with complete documentation including IFU and inventory list
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