06/15/2026
While we appreciate the communication from APIC to attendees on the trade show floor regarding Whole Room Microbial Reduction Devices, this category has been clearly defined by the FDA since 2023.
It is increasingly concerning to see manufacturers exhibit and market at national infection prevention conferences in the US trying to sidestep this regulatory requirement, whether by citing EPA registration or suggesting their devices avoid medical device surfaces.
In practice, non-critical medical device surfaces encompass the entire patient environment, including bedrails, IV poles, tray tables, nurse call buttons, sinks, toilets, door handles, workstations, and more. There is no alternative pathway for these claims in healthcare settings.
Find us at booth 1617 and learn more about the FDA’s QXJ category.