ObamaCare
Mandat Implan RFID dalam Semua rakyat Amerika (ObamaCare Mandates RFID Implants
in All Americans) . . .
GOVERNMENT
“EVIL’S WORK! (Kerja Iblis Kerajaan)! . . .
SitiWanMahani - 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"..
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" . . . 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?
It 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" . . .
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