FDA lists more guidance for SUDs (single-use devices) reprocessors
This article was originally published in Clinica
Reprocessors of single-use devices (SUDs) in the US now know when a simple label on a package will satisfy the US government's branding requirement for their products. Under the recently-enacted Medical Device User Fee Stabilization Act of 2005, all but reprocessors are exempt from having to brand their devices.
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