
Steris
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Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide is an FDA 510(k)-cleared medical device (K203223) manufactured by Steris. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 27, 2021. Regulation: 8.