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Dealing With Manufacturer’s Instructions for Use (IFUs) - 0.5 CE (for Central Sterile Techs)
5 days ago
The Food and Drug Administration requires that medical device manufacturers provide end-users in healthcare facilities with specific instructions for use (otherwise known as IFU) on how to clean and sterilize their products. This information should be obtained for every device processed at the facility and maintained in a binder. This course is offered through our partnership with course creator Nancy Chobin RN, AAS, ACSP, CFER, CSPM, who created this module for Sterile Processing University.
CBSPD APPROVAL CODE: # 1517KSWCOR19; Valid through: 5/1/2024 | IAHCSMM APPROVAL CODE: # 190805; Valid through: 5/8/2021
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