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Pentaferte S.P.A
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PENTATRASFU BLOOD TRANSFUSION SETS is an FDA 510(k)-cleared medical device (K041496) manufactured by Pentaferte S.P.A. 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 June 29, 2005. Regulation: 8.

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