IAHCSMM CRCST Practice Test – Chapter 12

IAHCSMM CRCST Practice Test – Chapter 12 (Certified Registered Central Service Technician) Practice Test Questions Answers online Quiz. n “IAHCSMM CRCST Practice Test Chapter 12: Assembly and Packaging,” readers will delve into the critical final steps of sterile processing in healthcare settings.

This chapter prepares them for the International Association of Healthcare Central Service Materiel Management (IAHCSMM) Certified Registered Central Service Technician (CRCST) exam, focusing on assembly and packaging of surgical instruments and other medical devices.

Readers will learn best practices for inspecting, assembling, and packaging these items to maintain sterility until use. The chapter includes practical scenarios, common pitfalls to avoid, and strategies to ensure patient safety and operational efficiency in the Sterile Processing Department. It also includes practice test questions to assess understanding and readiness for the CRCST certification.

IAHCSMM CRCST Practice Test – Chapter 12

Chapter 12

IAHCSMM CRCST Practice Test – Chapter 12

CRCST Practice Test
Chapter 12 Assembly and Packaging

Total Items: 43
Time Limit: N/A
Multiple Choice Quiz

1 / 43

Sequential wrapping techniques can be performed using which styles?

2 / 43

Which of the following is an advantage of sequential wrap over simultaneous wrap?

3 / 43

Why is it important to properly position paper-plastic peel pouches during sterilization?

4 / 43

What are the two basic types of combination peel pouches?

5 / 43

What is the most commonly used packaging material for small instruments and lightweight items?

6 / 43

What sterilization methods can craft paper pouches be utilized for?

7 / 43

What are pouches with both sides consisting of craft paper used for?

8 / 43

Which material should not be used as a packaging material for sterilization due to its tight weave?

9 / 43

What happens if the density of the packaging is too high for adequate sterile penetration?

10 / 43

What is one of the critical components to be inspected in a rigid sterilization container?

11 / 43

Which disadvantage of rigid container systems involves safety concerns?

12 / 43

How is the inspection of textile packaging performed?

13 / 43

The standards for manufacturing packaging materials have been based on which measurements?

14 / 43

What are the two basic types of reusable packaging material?

15 / 43

Packaging systems using healthcare facility-based sterilization are generally classified into:

16 / 43

Why should gauze sponges never be placed as additional packaging material in trays or packs?

17 / 43

What is the purpose of using tamper evidence seals on sterile packaging?

18 / 43

Why should heavier items be placed at the bottom of the tray?

19 / 43

How should items be arranged in the instrument trays for an emergency?

20 / 43

What are internal chemical indicators (CIs) used for?

21 / 43

What should be considered while packaging items for sterilization?

22 / 43

What is a "single instrument" in the context of this script?

23 / 43

What is a crucial aspect when preparing powered surgical instruments for sterilization?

24 / 43

Why should instrument substitutions not occur unless approved by the user department?

25 / 43

What is a key requirement during instrument assembling for procedure trays?

26 / 43

What does superheating refer to in the context of steam sterilization?

27 / 43

What is the major risk associated with overcrowding an instrument holding tray?

28 / 43

When should instruments be kept in an unlocked or open position?

29 / 43

What is the main concern when preparing basins for sterilization?

30 / 43

What should be done to protect the alignment of forceps tips?

31 / 43

What is the recommended maximum weight for containerized trays according to ANSI and AAMI ST77?

32 / 43

What is the primary purpose of demagnetizing surgical instruments?

33 / 43

When should instruments that have been disassembled for cleaning be reassembled and tested for proper function?

34 / 43

What should be done if a soiled instrument is detected during the inspection process?

35 / 43

What are some of the basic guidelines for instrument inspection during pack assembly?

36 / 43

What is one reason food and beverages are not allowed in the prep and pack area?

37 / 43

The cleanliness of the assembly area can be maintained by limiting traffic and controlling:

38 / 43

Which of the following best describes the role of positive air flow in the assembly area?

39 / 43

According to the provided information, why should nail polish and artificial nails not be worn in the prep impact area?

40 / 43

Relative humidity in the assembly area should be maintained between:

41 / 43

The correct temperature in the assembly area should be between:

42 / 43

The primary goals of creating an instrument pack are defined by the acronym FAN. What does FAN stand for?

43 / 43

Which of the following is NOT an objective of Chapter 12 "Assembly and Packaging"?

Your score is

See also: