BOTH HOUSE AND SENATE HEALTH BILLS REQUIRE THE MICRO CHIPPING OF
AMERICANS – 3/18/10
Required RFID implanted chip
Sec. 2521, Pg.
1000 – The government wil...l establish a National Medical Device Registry.
What does a National Medical Device Registry mean?

National
Medical Device Registry from H.R. 3200 [Healthcare Bill], pages
1001-1008:... See More(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.”Then on
page 1004 it describes what the term “data” means in paragraph 1,section
B:‘‘(B) In this paragraph, the term ‘data’ refers to information
respecting a device described in paragraph (1), including 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”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 it for yourself: http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm072191.pdf

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.Don’t believe
it? Look it up yourself. Healthcare Bill H.R. 3200: http://waysandmeans.house.gov/media/pdf/111/AAHCA09001xml.pdfPages 1001-1008
“National Medical Device Registry” section.Page 1006 “to be enacted
within 36 months upon passage”Page 503 “… medical device
surveillance”Why would the government use the word
“surveillance” when referring to citizens?

The definition of
“surveillance” is the monitoring of the behavior, activities, or other
changing information, usually of people and often in a secret manner.
The root of the word [French] means to “watch over.”See Morewww.fda.gov
www.fda.gov