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Teleflex, Inc.
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FLEXTIP PLUS CLOSED TIP EPIDURAL CATHERTER is an FDA 510(k)-cleared medical device (K103658) manufactured by Teleflex, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 15, 2012. Regulation: 8.