Hidden Obamacare Secret: "RFID Chip Implants" Mandatory for All by March 23, 2013
Republican
Congressman Ron Paul from Texas, states on his website:
"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........ He quotes that part of
the law and then goes on to say: "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
microchip for the purpose of controlling who is, or isn’t, allowed medical care
in their country".Read the
entire story at:
www.patriotactionnetwork.com/forum/topics/another-hidden-secret-inAnd now we
come to it. 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 them by now. I don’t want to discount them 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.This new 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 and tracking capability built into it.In just a
minute I’m going to show you the black and white of the law itself and you can
see it with your own eyes and wonder why an event of this magnitude which is
nothing less than seismic in nature is met with little more than silence in the
Christian community.Is it now
starting to dawn on you just where exactly we are in prophecy? I’ll ask that
question again in a minute and follow up on it, but now I want to show you the
law itself. I’ve downloaded a PDF copy of HR3200 from the government's website
so what I’m about to show you is from the bill itself its nothing that I’ve
written. You can access it all and see it all for yourself straight from the
source itself.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 postmarket
safety and outcomes data on each device that— ‘‘is or has 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.”What exactly
is a class II device that is implantable? As you saw earlier, it is the device
approved by the FDA in 2004.Federal
Food, Drug, and Cosmetic Act:www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuid...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."Going back
to what we just looked at, the creation of the national medical device registry
in section 2521, page 1002 line 5:“In
developing the registry, the secretary shall…”And the law
continues on with a laundry list of items that the secretary must do in the
process of creating this registry. In this laundry list of items to do, Line
17, subparagraph B: "validating methods for analyzing patient safety and
outcomes data from multiple sources and for linking such data with the
information included in the registry as described in subparagraph (A)"Going back
to subparagraph A [right above subparagraph B], it says: “including in the
registry, in a manner consistent with subsection (f), appropriate information
to identify each device described in paragraph (1) by type, model, and serial
number or other unique identifier;”Don’t be
confused by the intentional obfuscation and skillful wording, This law first
creates the national device registry and then immediately list all the task the
secretary of health and human services will have do in the process of creating
this registry.The very
first two items in the list mandates that the secretary first gives a unique
identification to each of the items listed in paragraph 1 which is:‘‘a class
III device; or ‘‘a class II device that is implantable.”Then, the
very next thing the secretary is to do is to create the process by which
“patient safety and outcomes data from multiple sources”, which is electronic
medical records, that are linked to these newly and uniquely identified items
from paragraph 1 which are the class III and class II implantable devices.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 can 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!Continuing a
few lines down in this same section, section B subsection ii on still on page
1002, the“patient safety and outcomes data from multiple sources”, that is to
be linked is clearly spelled out as electronic medical records. It reads: “link data obtained under clause (i) with
information in the registry”. Information in the registry is, as we know from
subparagraph A, the name of the device. So what is the data obtained under
clause i? Back up a few lines to clause iIt reads:
“obtain access to disparate sources of patient safety and outcomes data,
including Federal health-related electronic data”. Again, from breast implants,
to pacemakers, to RFID chips which one is the only possible one that can used
for the stated purpose in section B? That stated purpose is “for linking such
data” and the such data is electronic medical records.What we
already have already seen in just the creation of this registry, is the device
that will serve as the link, which is an RFID microchip that is categorized as
a Class II implantable device, as well as what it will be the link for which is
your electronic medical records.In case the
law wasn’t clear enough on that point, still in the laundry list of things to
do a few more lines down on the next page, page 1005“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." Now on Page 503, section E Lines 13-17 and I
quote: "encourage, as appropriate, the development and use of clinical
registries and the development of clinical effectiveness research data networks
from electronic health records, post marketing drug and medical device
surveillance efforts". Let me say that again, medical device surveillance
efforts!Now lets
look at section 163 of HR3200, which gives the government a direct electronic
access to your bank account which will work in conjunction with an implanted
chip.Page 58
Lines 5 through 15 reads:(D) enable
the real-time (or near real time) determination of an individual’s financial
responsibility at the point of service and, to the extent possible, prior to
service, including whether the individual is eligible for a specific service
with a specific physician at a specific facility, which may include utilization
of a machine-readable health plan beneficiary identity detection card; (E)
enable, where feasible, near real-time adjudication of claimsWhat does
this mean? It means that the government will give everybody a health ID card
that contains a machine readable device (magnetic strip or RFID chip) similar
to a credit card. Embedded in this chip or strip is your Health Identification
Number. When you visit a medical provider, the medical claims will be processed
while you are still in the office. The medical providers will be paid in real
time. The portion that you owe will be deducted from your bank account, in real
time, according to HR 3200.READ MORE
http://members.beforeitsnews.com/story/665/502/Hidden_Obamacare_Secret:_RFID_Chip_Implants_Mandatory_for_All_by_March_23%2c_2013.html
UPDATE!!!Revised
version ALSO has RFID requirement!!!read more
http://ppsimmons.blogspot.ca/2012/07/marl-of-beast-watch-obamacare-to-track.html
Not in me.
ReplyDeleteThere are a lot of reasons to oppose the Obamacare bill but this is not one of them because it's not true.
ReplyDeleteThis rumor was based on a preliminary version of the bill, HR 3200. The bill was amended several times since then and the version passed by Congress, HR 3590, doesn't contain the provision mentioned in this article. There is no subtitle C, Section 2521 in the bill. I've got the text of this bill in a PDF document and did a search for that section and it's not there. There's also no mention in the final bill of "implantable" devices.
The revised version ALSO has the RFID requirement...
Deletehttp://ppsimmons.blogspot.ca/2012/07/marl-of-beast-watch-obamacare-to-track.html
By the way, here's a link to the text of the final bill. http://www.gpo.gov/fdsys/pkg/BILLS-111hr3590enr/pdf/BILLS-111hr3590enr.pdf
ReplyDeleteThe revised version ALSO has the RFID requirement...
Deletehttp://ppsimmons.blogspot.ca/2012/07/marl-of-beast-watch-obamacare-to-track.html
The revised version ALSO has the RFID requirement...
ReplyDeletehttp://ppsimmons.blogspot.ca/2012/07/marl-of-beast-watch-obamacare-to-track.html
It dont make much sense, how can they get the chip in every single American as soon as March 23? I thought the law didnt even go into effect until 2014.
ReplyDelete