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Microchiping included in Healthcare Bill ? "Buried deep within the over 1,000 pages of the massive US Health Care Bill (PDF) in a “non-discussed” section titled: Subtitle C-11 Sec. 2521— National Medical Device Registry, and which states its purpose as:
“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; and ‘‘(B) is a class III device; or ‘‘(ii) a class II device that is implantable.”
In “real world speak”, according to this report, this new law, when fully implemented, provides the framework for making the United States the first Nation in the World to require each and every one of its citizens to have implanted in them a radio-frequency identification (RFID) microchip for the purpose of controlling who is, or isn’t, allowed medical care in their country.
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Healthcare Bill H.R. 3200:
http://waysandmeans.house.gov/media/pdf/111/AAHCA09001xml.pdf Pages 1001-1008 “National Medical Device Registry” section.
Page 1006 “to be enacted within 36 months upon passage”
Page 503 “… medical device surveillance”
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What exactly is a class II device that is implantable?
Approved by the FDA, a class II implantable device is an “implantable radio frequency transponder system for patient identification and health information.” The purpose of a class II device is to collect data in medical patients such as “claims data, patient survey data, standardized analytic files that allow for the pooling and analysis of data from disparate data environments, electronic health records, and any other data deemed appropriate by the Secretary.”
See: http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/Guidance...
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