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Medos International SARL
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CODMAN CERTAS PROGRAMMABLE VALVE SYSTEM, CODMAN CERTAS THERAPY MANAGEMENT SYSTEM is an FDA 510(k)-cleared medical device (K112156) manufactured by Medos International SARL. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 16, 2011. Regulation: 8.