Do Not Inject Me ! Say No To Vaccines

'Buried deep within the over 1,000 pages of the massive US Health Care Bill (PDF) in a 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; (B) is a class III device; or 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.'

Sec. 2521, Pg. 1000 – The government will establish a National Medical Device Registry.

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.”

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: 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.

See 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”

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.”

In theory, the intent to streamline healthcare and to eliminate fraud via “health chips” seems right. But, to have the world’s lone superpower (America, for now) mandate (page 1006) a device to be IMPLANTED is scary!

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