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IN THE UNITED STATES DISTRICT COURT FOR THE SOUTHERN DISTRICT OF WEST VIRGINIA CHARLESTON DIVISION IN RE: C.R. BARD, INC., PELVIC REPAIR SYSTEM PRODUCTS LIABILITY LITIGATION MDL 2187 THIS DOCUMENT
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CR Bard Inc Pelvi refers to a medical device manufacturer that produces pelvic mesh implants.
Healthcare providers and facilities that use or implant CR Bard Inc Pelvi devices are required to file reports.
The CR Bard Inc Pelvi reports can be filled out online through the FDA's Manufacturer and User Facility Device Experience Database (MAUDE) system.
The purpose of CR Bard Inc Pelvi reports is to track any adverse events or complications associated with the use of the pelvic mesh implants.
Information such as patient demographics, details of the implant procedure, any adverse events or complications, and follow-up outcomes must be reported on CR Bard Inc Pelvi.
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