CDA · 8% of the exam
ICE: Process Instruments and Devices practice questions
10 free ICE: Process Instruments and Devices questions for the Certified Dental Assistant (CDA) Exam exam, each with the correct answer and an explanation for every option.
What this domain covers
Reprocessing reusable instruments from the point of use to storage: cleaning, packaging, sterilisation and monitoring.
- Exam weight
- 8%
- On a real exam
- ≈ 20 questions
- In our bank
- 51 questions
Topics that come up most
- Spaulding classification: critical, semi-critical, non-critical
- Ultrasonic cleaning and instrument washers
- Sterilisation methods and cycle parameters
- Mechanical, chemical and biological monitoring
- Packaging, storage and handling a failed spore test
How to study it
Learn what each type of indicator tells you and how often biological monitoring is done; questions often ask what to do when a test fails.
Sample ICE: Process Instruments and Devices questions
Try each one before opening the answer. Original questions written to the official exam objectives.
Question 1
Why should instrument cassettes be wrapped in packaging made for sterilization before they are placed in the sterilizer?
- AThe wrap keeps the instruments sterile after the cycle until the package is opened for use
- BThe wrap keeps steam off the instrument surfaces so the instruments do not corrode
- CThe wrap replaces the need for an internal chemical indicator inside the cassette
- DThe wrap lets cassettes be sterilized safely even if the debris was not fully cleaned off first
Show answer and explanation
Answer: A) The wrap keeps the instruments sterile after the cycle until the package is opened for use
Sterilization packaging must let the sterilant reach the instruments and then keep them sterile until the package is opened. Wrapping does not replace cleaning or internal chemical indicators.
- ACorrect. CDC says packaging materials must let the sterilizing agent penetrate and must keep items sterile after sterilization until the point of use.
- BIncorrect. Sterilization wraps must let steam or another sterilant reach the instruments. If the wrap blocked steam, the instruments would not be sterilized.
- CIncorrect. CDC calls for an internal chemical indicator in every package. Wrapping does not replace it.
- DIncorrect. Instruments must be cleaned before packaging and sterilization. Leftover debris can shield microorganisms from the sterilant, and wrapping does not make up for poor cleaning.
Question 2
An assistant packs the ultrasonic cleaner basket tightly so a large batch of instruments can be processed at once. What is the main problem with this practice?
- ACrowded instruments can keep the solution's cavitation from reaching every surface
- BA heavy load lowers the solution temperature below the level needed to sterilize
- CExtra instruments intensify cavitation enough to pit and dull cutting edges
- DLarge loads neutralize the solution's disinfectant, which is what removes debris
Show answer and explanation
Answer: A) Crowded instruments can keep the solution's cavitation from reaching every surface
Ultrasonic cleaners remove debris through cavitation in the solution. Overloading keeps the solution from reaching all instrument surfaces and reduces cleaning.
- ACorrect. Ultrasonic cleaning removes debris through cavitation in an aqueous solution. Instruments packed tightly together shield one another, so some surfaces are not cleaned.
- BIncorrect. An ultrasonic cleaner cleans instruments; it does not sterilize them. Sterilization happens later in the process.
- CIncorrect. Overloading reduces cleaning effectiveness. It does not intensify cavitation.
- DIncorrect. Debris is removed mainly by cavitation. CDC notes that typical ultrasonic solutions often carry no antibacterial label claims.
Question 3
When are handpieces lubricated?
- AOnly after a patient complains about noise or vibration
- BNever
- CBefore sterilization, as the manufacturer directs
- DAfter use on the next patient
Show answer and explanation
Answer: C) Before sterilization, as the manufacturer directs
- AIncorrect. Lubricate routinely.
- BIncorrect. Many need lubrication.
- CCorrect. Some need lubrication after as well.
- DIncorrect. Lubricate before sterilizing.
Question 4
Wrapped packages should be removed from a steam sterilizer:
- AImmediately while wet
- BAfter they dry
- CBefore the cycle ends
- DThe next week
Show answer and explanation
Answer: B) After they dry
- AIncorrect. Let them dry first.
- BCorrect. Wet packs can wick in contamination.
- CIncorrect. Let the cycle and drying finish.
- DIncorrect. Remove them after drying.
Question 5
When loading a sterilizer, packages should be:
- ALeft unwrapped always
- BPacked tightly together to save cycles
- CStacked flat in piles
- DPlaced loosely, not overloaded
Show answer and explanation
Answer: D) Placed loosely, not overloaded
- AIncorrect. Package per protocol.
- BIncorrect. That blocks circulation.
- CIncorrect. That blocks circulation.
- DCorrect. So sterilant can circulate.
Question 6
Which storage practice for sterilized instrument packages is consistent with CDC recommendations?
- AKeep them in covered or closed cabinets in an area where they cannot become wet
- BKeep them on open shelves directly above the sterilization-area sink for quick access
- CKeep a supply on the operatory counter, uncovered, so they are ready for each patient
- DStore them in any cabinet, and use packages that got damp as long as they are within the date
Show answer and explanation
Answer: A) Keep them in covered or closed cabinets in an area where they cannot become wet
CDC recommends storing sterile packages in covered or closed cabinets away from water. Packages that become wet, torn, or punctured must be reprocessed before use.
- ACorrect. CDC says sterile instruments and supplies should be stored in covered or closed cabinets and not where they might become wet.
- BIncorrect. Storing packages near a sink exposes them to splashes. Wet packages are considered contaminated and must be reprocessed.
- CIncorrect. An uncovered operatory counter exposes packages to spatter and handling. CDC recommends covered or closed cabinets.
- DIncorrect. Packages must be inspected before use, and any that are wet, torn, or punctured must be reprocessed no matter what date is on them.
Question 7
A dental practice uses event-related shelf life for its sterilized instrument packages. Under this practice, a stored package should be considered sterile until:
- AThe package is torn, gets wet, or has its seal broken
- BThe expiration date printed on the label, typically 30 days after processing
- CThe sterilizer's next weekly biological indicator test is completed
- DThe chemical indicator on the package begins to fade during storage
Show answer and explanation
Answer: A) The package is torn, gets wet, or has its seal broken
Event-related shelf life means a sterile package stays usable until an event compromises it, such as tearing, moisture or a broken seal, rather than until a set date. Packages should be inspected for damage before use.
- ACorrect. Under event-related practice, an item stays sterile until something contaminates it, such as a tear, moisture or a broken seal. The package must be inspected before use.
- BIncorrect. A fixed expiration date describes time-related shelf life, not event-related shelf life.
- CIncorrect. Spore testing checks how the sterilizer is performing. It does not set how long an already-processed package stays sterile.
- DIncorrect. A chemical indicator shows that the package was exposed to sterilization conditions. Its appearance during storage is not what ends sterility under event-related practice.
Question 8
After instruments have been cleaned and rinsed, what should happen before they are wrapped or placed in sterilization pouches?
- APackage them right away, since the sterilizer's heat will dry them during the cycle
- BAllow them to dry thoroughly, then inspect them before packaging
- CLeave them damp from rinsing so steam can reach their surfaces more easily
- DReturn them to a holding solution until the sterilizer is ready for the next load
Show answer and explanation
Answer: B) Allow them to dry thoroughly, then inspect them before packaging
CDC directs that cleaned instruments be dried thoroughly before packaging, because moisture compromises the wrap or pouch and its ability to keep the contents sterile.
- AIncorrect. CDC says instruments should dry thoroughly before packaging. Moisture can compromise the packaging and its ability to keep the contents sterile.
- BCorrect. CDC directs that cleaned instruments be allowed to dry thoroughly before they are packaged, wrapped, or otherwise contained, and that they be inspected first.
- CIncorrect. Leftover water does not help steam reach the instruments. Wet instruments can damage the integrity of the packaging material.
- DIncorrect. A holding solution is used before cleaning to keep debris from drying on. Instruments that have been cleaned and rinsed should be dried and packaged, not soaked again.
Question 9
What is a typical prevacuum steam cycle?
- AAbout 270°F (132°C) for about 4 minutes
- BAbout 212°F for 4 hours
- CAbout 400°F for 1 minute
- DAbout 100°F for 30 minutes
Show answer and explanation
Answer: A) About 270°F (132°C) for about 4 minutes
- ACorrect. Air is removed before steam enters.
- BIncorrect. That's too low.
- CIncorrect. That's too high for steam.
- DIncorrect. That's far too low.
Question 10
A common steam autoclave cycle runs at about:
- A500°F (260°C)
- B150°F (66°C)
- C212°F (100°C)
- D250°F (121°C)
Show answer and explanation
Answer: D) 250°F (121°C)
- AIncorrect. That's far too hot for steam.
- BIncorrect. That's too cool to sterilize.
- CIncorrect. That's boiling, not sterilization.
- DCorrect. For about 30 minutes, or hotter for shorter cycles.
ICE: Process Instruments and Devices: FAQs
How much of the CDA exam is ICE: Process Instruments and Devices?
ICE: Process Instruments and Devices is 8% of the CDA exam by the official exam guide's weighting, which on a 245-question form works out to roughly 20 questions. The real exam's exact split varies by form.
What does the ICE: Process Instruments and Devices domain cover?
Reprocessing reusable instruments from the point of use to storage: cleaning, packaging, sterilisation and monitoring.
How should I study ICE: Process Instruments and Devices for CDA?
Learn what each type of indicator tells you and how often biological monitoring is done; questions often ask what to do when a test fails.
Where can I practise more ICE: Process Instruments and Devices questions?
This page has 10 free ICE: Process Instruments and Devices questions with answers. The ExamWize CDA question bank has 51 questions in this domain. Every practice exam result breaks your score down by domain, and Review Mode re-drills the questions you missed.
Other CDA topics
- GC: Evaluation7% of the exam
- GC: Patient Management and Administration7% of the exam
- GC: Chairside Dentistry19% of the exam
- GC: Dental Materials6% of the exam
- ICE: Prevention of Disease Transmission6% of the exam
- ICE: Prevention of Cross-contamination10% of the exam
- ICE: Occupational Safety and Administration Protocols6% of the exam
- RHS: Purpose and Technique15% of the exam
- RHS: Radiation Characteristics and Protection8% of the exam
- RHS: Infection Prevention and Control8% of the exam
Also: 15 free questions across all topics, the CDA cheat sheet and the study guide.
Get ICE: Process Instruments and Devices exam-ready
The full CDA bank has 51 ICE: Process Instruments and Devices questions. Timed practice exams match the real exam's length and domain weights, every result shows your score per domain, and Review Mode re-drills the questions you missed.
Not affiliated with DANB; questions are original, written from the official exam outline, and never copied from the real exam.