Real‐world experience of suture‐based closure devices: Insights from the FDA Manufacturer and User Facility Device Experience
Sign Up to like & getrecommendations! Published in 2021 at "Catheterization and Cardiovascular Interventions"
DOI: 10.1002/ccd.29501
Abstract: We analyzed post‐marketing surveillance data from the United States Food and Drug Administration (FDA) Manufacturer and User Facility Device Experience (MAUDE) database for suture‐based vascular closure devices (VCDs) – Perclose ProGlide (Abbott, Chicago, Illinois) and… read more here.
Keywords: fda manufacturer; user facility; facility device; manufacturer user ... See more keywords
A comprehensive analysis of MRI‐related Cochlear implant adverse events reported by FDA's manufacturer and user facility device experience database
Sign Up to like & getrecommendations! Published in 2025 at "Laryngoscope Investigative Otolaryngology"
DOI: 10.1002/lio2.70073
Abstract: Identify MRI‐related cochlear implant (CI) adverse events from the Food and Drug Administration (FDA) Manufacturer and User Facility Device Experience (MAUDE) database and determine whether devices with diametric magnets are associated with reduced adverse events. read more here.
Keywords: adverse events; fda manufacturer; cochlear implant; mri related ... See more keywords