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Business · 29/11/2016

FDA Releases Guidance on Reducing Cross-Contamination Risk with Flexible Gastrointestinal Endoscopes

The Food and Drug Administration (FDA) has published guidance to help mitigate the risk of cross-contamination from valves and accessories used in flexible gastrointestinal endoscopes, a class II medical device, during procedures such as colonoscopies.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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