Universal Digital Interface 2W, UDI 2W

Universal Digital Interface 2W, UDI 2W is an FDA 510(k)-cleared medical device (K143232) manufactured by Meridian Medical Systems, LLC. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 29, 2015. Regulation: 8.