Following manufacturers’ instructions for use (IFU) is among the most important responsibilities of the Sterile Processing (SP) team, and every item in our departments has an IFU—surgical instruments, processing equipment, detergents, disinfectants, and cleaning tools. Although critical for device care and patient safety, IFU do not have a standardized format or common layout. Each document looks different, which can make the process of trying to follow IFU feel Intense, Frustrating and Unclear.

In episode 128, host Jon Wood speaks with Randalyn Harreld of SteelcoBelimed about decoding IFU. Harreld describes most IFU as having “endless amounts of information.” In addition to the cleaning and sterilization sections, she identifies key components of IFU, including contraindications, preparation for use, and handling and storage. Harreld explains the term “compatibility matrix” and the differences between verification and validation. She also emphasizes the importance of looking for and following all cautions and warnings. Finally, Harreld offers strategies for housing and managing access to IFU. Listen in to learn how to better understand—and properly use—your IFU.

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