National Medical Device Registry from H.R. 3200 [Healthcare Bill], pages 1001-1008: (g)(1) The Secretary shall establish a national medical device registry (in this subsection referred to as the ‘registry’) to facilitate analysis of postmarket safety and outcomes data on each device that— ‘‘(A) is or has been used in or on a patient; ‘‘(B)and is— ‘‘(i) a class III device; or ‘‘(ii) a class II device that is implantable, life-supporting, or life-sustaining.”.... google subtitle c-11 sec. 2521 they wanna chip us .....
Posted on: Tue, 01 Oct 2013 22:31:39 +0000
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