(Subtitle C-11 Sec. 2521 National Medical Device Registry), but maybe you can tell me what it means.

"... 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 that has been used in or on a patient; and (B) is a Class III device; or (ii) A Class II device that is Implantable..."

Well, enough of that, a person can take only so much nonsense at one sitting. But, ask yourself a simple question: Are we to be multi-chipped, complete with updates, like a computer program, with our yearly rounds of multi-inoculations?

[link to rense.com]