Another hidden secret in Obamacare - “RFID Chip Implants

Please prove this wrong!

 

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Saturday, March 10, 2012 Another hidden secret in Obamacare - “RFID Chip    Implants”

Another hidden secret in    Obamacare - “RFID Chip    Implants”

Are you ready to have your RFID Chip    Implanted ?

3/23/2013 is your    date!

By Fred Brownbill on February 14, 2012 in Constitution Legal    Watch

This new    Health Care (Obamacare) law requires an RFID chip implanted in all of us. This    chip will

not only    contain your personal information with tracking capability but it will also be    linked to your

bank    account. And..... get this, Page 1004 of the new law    (dictating the timing of this chip)reads and I quote: "Not later than 36    months after the date of the enactment."

It is now the law of the land    that by March 23rd 2013 we will all be required to have an RFID    chip underneath our skin and this    chip will be link to our bank accounts as well as have our personal records    a nd tracking capability built    into it.

http://polidics.com/news/    another-hidden-secret-in- obamacare-rfid-chip-implants.    html

On    Sunday March 21, 2010 the Senate Healthcare bill HR3200 was passed and signed    into law the f ollowing Tuesday. Page 1004 of the new law    (dictating the timing of this chip), reads, and I quote:

“Not    later than 36 months after the date of the enactment” H.R. 3200 section 2521,    Pg. 1001, paragraph 1.

“The    Secretary shall establish a national medical device registry (in this    subsection referred to as the ‘registry’) to facilitate analysis of    post-market safety and outcomes data on each device that— ‘‘is or    h as been used in or on a patient; ‘‘and is—    ‘‘a class III device; or ‘‘a class II device that is implantable, life-supporting, or    life-sustaining.”

Federal Food, Drug, and Cosmetic    Act:

http://www.fda.gov/downloads/    MedicalDevi%E2%80%A6

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 s uch as “claims data, patient survey data,    and standardized analytic files that allow for the pooling and analysis of data from disparate data    environments, electronic health records, and any other data    d eemed appropriate by the    Secretary.”

Class III    devises are items such as breast implants, pacemakers, heart valves,    etc.

A Class    II device that is implantable is, as you seen from    the FDA, an implantable radio frequency transponder, RFID chip. From breast implants, to pacemakers,    to RFID chips which one is the only possible one that c an used    for the stated purpose in section B which is, “for linking such data with the    information included in the    registry”? As we know from subsection A, the information in the registry is    the name of a device. In plain speak, we are in a clear    way being told that our electronic medical records are going to be linked to a class II implantable    device!

On Sunday March    21, 2010 the Senate Healthcare bill HR3200 was passed and    signed into law the following Tuesday. Like I said before, there are a    legion of horrible and just plain evil aspects to this bill and I’m sure    you’ve heard a lot of them by now. I don’t want to discount    t hem but what    cannot be missed here is this new law now opens a    prophetic door on a magnitude not seen since the reformation of    Israel.

“The    Secretary to protect the public health; shall establish procedures to permit    linkage of information submitted pursuant to subparagraph (A,    remember subparagraph A is the class 2 implantable device    reference) with patient safety and outcomes data obtained under paragraph (3,    which is electronic medical records); and to permit analyses of    linked data;”

Continuing on to page 1007, in the    STANDARDS, IMPLEMENTATION CRITERIA, AND CERTIFICATION CRITERIA    section, the secretary of health and human services is given full power to    intact all mandates from the laundry list of to-do    items in the creation process of the registry as well as dictate how the devises listed in the National    Medical Device Registry are to be used and implemented.

“The    Secretary of the Health Human Services, acting through the head of the Office    of the National Coordinator for Health Information    Technology, shall adopt standards, implementation    specifications, and certification criteria for the    electronic exchange and use in certified electronic health records of a unique device identifier for each    device described in paragraph 1 (National Medical Device Registry), if such an identifier is    required by section 519(f) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360i(f)) for the    device.”