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S1039 Adverse Events Associated with the Use of FDA-Approved Innovative Duodenoscope Designs: An Analysis of Medical Device Reports (MDRs) from the Manufacturer and User Facility Device Experience (MAUDE) Database. (October 2021)
Record Type:
Journal Article
Title:
S1039 Adverse Events Associated with the Use of FDA-Approved Innovative Duodenoscope Designs: An Analysis of Medical Device Reports (MDRs) from the Manufacturer and User Facility Device Experience (MAUDE) Database. (October 2021)
Main Title:
S1039 Adverse Events Associated with the Use of FDA-Approved Innovative Duodenoscope Designs: An Analysis of Medical Device Reports (MDRs) from the Manufacturer and User Facility Device Experience (MAUDE) Database