OEM Industry Eager For FDA Determination On Reuse Of Single-Use Devices
This article was originally published in The Gray Sheet
Executive Summary
FDA should set "timeframes" by which reprocessors of single-use devices must submit data to the agency showing that the devices are safe when reused, Stephen Northrup, executive director of the Medical Device Manufacturers Association, said at a May 6 conference on reuse of single-use devices in Arlington, Virginia.
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