TIDI BRAND STERILIZATION WRAP

TIDI BRAND STERILIZATION WRAP is an FDA 510(k)-cleared medical device (K042580) manufactured by Banta Healthcare Group, Ltd.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 16, 2004. Regulation: 8.