
Medi-Globe Corp.
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GIP/MEDI-GLOBE GUIDE WIRES & WIND-UP GUIDE WIRES is an FDA 510(k)-cleared medical device (K941973) manufactured by Medi-Globe Corp.. 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 June 29, 1995. Regulation: 8.