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Covidien Lp, Formerly Registered AS United States
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AUTOSUTURE VERSAPORT PLUS BLADLESS TROCAR; BLADELESS TROCAR is an FDA 510(k)-cleared medical device (K081169) manufactured by Covidien Lp, Formerly Registered AS United States. 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 May 22, 2008. Regulation: 8.

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