Refresher #2

Front

The US FDA is responsible for:
- Maintaining all manufacturer records
- Ensuring items can be properly cleaned and sterilized
- Monitoring the high level disinfection process
- Ensuring cleaning chemicals are safe

Back

Ensuring items can be properly cleaned and sterilized

Front

Aseptic technique is knowing the

Back

activities that prevent infection

Front

the decontamination area of SPD should have

Back

negative airflow

Front

Proper handling of instrumentation is the responsibility of:

• the surgeon
• the scrub tech
• the Sterile Tech
• everybody who comes in contact with the instrumentation

Back

everybody who comes in contact with the instrumentation

Front

What does the Center for Disease Control and Prevention (CDC) do?

Back

Responds to health emergencies

Front

The federal program designed for the voluntary reporting of device related problems is called

Back

MedWatch

Front

When removing PPE, first remove: gloves, gown, mask, shoe covers

Back

shoe covers

Front

What tells the primary meaning of a word?

Back

Root word element

Front

In SP, the concept of "one way flow of materials" refers to the movement of products.

Back

from soiled processing areas to clean processing areas within SPD

Front

Traffic control/dress code requirement for clean assembly area of SPD: biohazard, unrestricted, semi-restricted, restricted.

Back

semi-restricted