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Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!

 
The White House
User ID: 799732
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11/20/2009 01:49 PM
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Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
Jack be nimble,

Jack be quick.

"What the Fuck's up with this micro-chip?"

Subtitle C-11 Sec. 2521 National Medical Device Registry

"... 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 that has been used in or on a patient; and (B) is a Class III device; or (ii) A Class II device that is Implantable..."
[link to www.rense.com]
Anonymous Coward
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11/20/2009 01:51 PM
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bsflag
Anonymous Coward
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11/20/2009 01:57 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
Jack be nimble,

Jack be quick.

"What the Fuck's up with this micro-chip?"

Subtitle C-11 Sec. 2521 National Medical Device Registry

"... 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 that has been used in or on a patient; and (B) is a Class III device; or (ii) A Class II device that is Implantable..."
[link to www.rense.com]
 Quoting: The White House 799732

You, sir, are a fucking nitwit!
A medical device is something doctors use to facilitate examinations ie. x-ray machines, ekg machines, mri machines, thermometers they stick up YOUR ASS, and other things like that. It takes a feeble mind to make the jump from medical devices to micro-chips. Put the bong down and stop buying that shit off the streets. Learn to grow your own.
The White House (OP)
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11/20/2009 01:59 PM
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The registry already exists for heart pumps and isulin pumps ect. But the vague langauge at this point in the bill not only specifies Class II and Class III but any implant the Secretary chooses to include.

All these things are "good" ideas. The need to track implantable devices in case there is a recall or multiple failures beginning to occur or other medical complications. It is when language gets slipped into a good idea that leaves it vague and open ended that we have a trojan horse of anything any adminstration chooses to dump into it.

Is the verichip a "wonderful" and "logical" idea whose time has come?
The White (OP)
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11/20/2009 02:01 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
In “real world speak”, 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.

It goes without saying, of course, that this new “Med-Chip” these American’s will be forced to have put inside them will not only control their access to medical resources, but will also enable their government to know their whereabouts, spending habits, and so much more as to effectively make these people nothing more than “human cattle” to be herded, controlled, and if they object to their new status, led to the slaughterhouse.
Anonymous Coward
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11/20/2009 02:04 PM
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Why is this crap pinned?

bsflag
The White House (OP)
User ID: 799732
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11/20/2009 02:06 PM
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The Language is crystal clear!

You will bend over!


National Medical Device Registry
(g)(1) The Secretary shall establish a national med-
ical 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; and ‘‘(B) is—
(i) a class III device; or
(ii) a class II device that is implantable,
life-supporting, or life-sustaining.
(2) In developing the registry, the Secretary shall,
in consultation with the Commissioner of Food and Drugs,
the Administrator of the Centers for Medicare & Medicaid
Services, the head of the Office of the National Coordi-
nator for Health Information Technology, and the Sec-
retary of Veterans Affairs, determine the best methods
for— ‘‘(A) including in the registry, in a manner con-
sistent with subsection (f), appropriate information
to identify each device described in paragraph (1) by
type, model, and serial number or other unique iden-
tifier;
(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), in-
cluding, to the extent feasible, use of—
(i) data provided to the Secretary under
other provisions of this chapter; and ‘‘(ii) information from public and private
sources identified under paragraph (3); ‘‘(C) integrating the activities described in this
subsection with—
(i) activities under paragraph (3) of sec-
tion 505(k) (relating to active postmarket risk
identification);
(ii) activities under paragraph (4) of sec-
tion 505(k) (relating to advanced analysis of
drug safety data); and
(iii) other postmarket device surveillance
activities of the Secretary authorized by this
chapter; and
(D) providing public access to the data and
analysis collected or developed through the registry in a manner and form that protects patient privacy
and proprietary information and is comprehensive,
useful, and not misleading to patients, physicians,
and scientists.
(3)(A) To facilitate analyses of postmarket safety
and patient outcomes for devices described in paragraph
(1), the Secretary shall, in collaboration with public, aca-
demic, and private entities, develop methods to—
(i) obtain access to disparate sources of
patient safety and outcomes data, including—
(I) Federal health-related electronic
data (such as data from the Medicare pro-gram under title XVIII of the Social Secu-
rity Act or from the health systems of the
Department of Veterans Affairs);
(II) private sector health-related
electronic data (such as pharmaceutical
purchase data and health insurance claims
data); and
(III) other data as the Secretary
deems necessary to permit postmarket as-
sessment of device safety and effectiveness;
and
(ii) link data obtained under clause (i) with information in the registry.
(B) In this paragraph, the term ‘data’ refers to in-
formation 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.
(4) Not later than 36 months after the date of the
enactment of this subsection, the Secretary shall promul-
gate regulations for establishment and operation of the
registry under paragraph (1). Such regulations— ‘‘(A)(i) in the case of devices that are described
in paragraph (1) and sold on or after the date of the
enactment of this subsection, shall require manufac-
turers of such devices to submit information to the
registry, including, for each such device, the type,
model, and serial number or, if required under sub-
section (f), other unique device identifier; and
(ii) in the case of devices that are described in
paragraph (1) and sold before such date, may re-
quire manufacturers of such devices to submit such
information to the registry, if deemed necessary by
the Secretary to protect the public health;
(B) shall establish procedures— ‘‘(i) to permit linkage of information sub-
mitted pursuant to subparagraph (A) with pa-
tient safety and outcomes data obtained under
paragraph (3); and
(ii) to permit analyses of linked data;
(C) may require device manufacturers to sub-
mit such other information as is necessary to facili-
tate postmarket assessments of device safety and ef-
fectiveness and notification of device risks;
(D) shall establish requirements for regular
and timely reports to the Secretary, which shall be
included in the registry, concerning adverse event trends, adverse event patterns, incidence and preva-
lence of adverse events, and other information the
Secretary determines appropriate, which may include
data on comparative safety and outcomes trends;
and
(E) shall establish procedures to permit public
access to the information in the registry in a manner
and form that protects patient privacy and propri-
etary information and is comprehensive, useful, and
not misleading to patients, physicians, and sci-
entists.
(5) To carry out this subsection, there are author-ized to be appropriated such sums as may be necessary
for fiscal years 2010 and 2011.’’.
(2) EFFECTIVE DATE.—The Secretary of
Health and Human Services shall establish and
begin implementation of the registry under section
519(g) of the Federal Food, Drug, and Cosmetic
Act, as added by paragraph (1), by not later than
the date that is 36 months after the date of the en-
actment of this Act, without regard to whether or
not final regulations to establish and operate the
registry have been promulgated by such date.
(3) CONFORMING AMENDMENT.—Section
303(f)(1)(B)(ii) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 333(f)(1)(B)(ii)) is amend-
ed by striking ‘‘519(g)’’ and inserting ‘‘519(h)’’.
(b) ELECTRONIC EXCHANGE AND USE IN CERTIFIED ELECTRONIC HEALTH RECORDS OF UNIQUE DEVICE
IDENTIFIERS.—
(1) RECOMMENDATIONS.—The HIT Policy
Committee established under section 3002 of the
Public Health Service Act (42 U.S.C. 300jj–12)
shall recommend to the head of the Office of the Na-
tional Coordinator for Health Information Tech-
nology 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 section
519(g)(1) of the Federal Food, Drug, and Cosmetic
Act, as added by subsection (a).
(2) STANDARDS, IMPLEMENTATION CRITERIA,
AND CERTIFICATION CRITERIA.—The Secretary of
the Health Human Services, acting through the
head of the Office of the National Coordinator for
Health Information Technology, shall adopt stand-
ards, implementation specifications, and certification
criteria for the electronic exchange and use in cer-
tified electronic health records of a unique device
identifier for each device described in paragraph (1),
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.
The White House (OP)
User ID: 799732
United States
11/20/2009 02:15 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
included in the Stimulus Bill was already a plan to convert our medical records into Electronic Health Records (EHR). The H.R. 3200 is just another stone in the foundation that has been layed.

From my understanding, once the ground work is setup in the hospitals to make them all electronic, then this Act could be changed or ammended or another bill swept through in the future to upgrade our machine-readable identification cards to implantable RFID chips...at the Sectretary's discretion...based on the data he/she collects on the reliability, etc. of such a device.

At some point in the future, in order to recieve health care, and eventually we all need to see a doctor, we theoratically would have to be chipped.
The White House (OP)
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11/20/2009 02:17 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
The Food and Drug Administration (FDA) is classifying the implantable radiofrequency transponder system for patient identification and health information into class II (special controls).

The special control that will apply to the device is the guidance document entitled ``Class II Special Controls Guidance Document: Implantable Radiofrequency Transponder System for Patient Identification and Health Information.
Anonymous Coward
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11/20/2009 02:18 PM
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I'm already working on hacking the RF chip. Should be easy enough. A combo of RF remote hacks and wifi encription should be all that is needed. I'm just hoping there is SSNs in the chip... Easy as pie...
Anonymous Coward
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11/20/2009 02:18 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
What is the class III device?
Anonymous Coward
User ID: 809505
Canada
11/20/2009 02:19 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
Oh come on, this is bottom of the barrel.

bsflag
PACNWguy

User ID: 688273
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11/20/2009 02:19 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
After the royal ass fucking we are getting from the Dildo Obama, there will be plenty of room to insert chips.
OBAMA - THE FASTEST FAILED PRESIDENT IN AMERICAN HISTORY

"I inherated and I am Great!"
The White House (OP)
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11/20/2009 02:19 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
From the Class II Special Controls Guidance Document link above...

2. Scope
The scope of this document is limited to the following device as described in 21 CFR 880.6300 Implantable Radiofrequency Transponder System for Patient Identification and Health Information (product code: NRV):
An implantable radiofrequency transponder system for patient identification and health information is a device intended to enable access to secure patient identification and corresponding health information. This system may include a passive implanted transponder, inserter, and scanner. The implanted transponder is used only to store a unique electronic identification code which is read by the scanner. The identification code is used to access patient identity and corresponding health information stored in a database.
Anonymous Coward
User ID: 703397
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11/20/2009 02:21 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
a "class II implantable device." I'm trying to figure out what that means:

[link to www.fda.gov]

From the link above (btw, this doesn't sound like a pacemaker to me) "This guidance document was developed as a special control guidance to support the
classification of the implantable radiofrequency transponder system for patient identification and
health information into class II (special controls). The device is intended to enable access to
secure patient identification and corresponding health information in humans. This guidance is
issued in conjunction with a Federal Register notice announcing the classification of implantable
radiofrequency transponder system for patient identification and health information."

Here is what I'm learning about a "class III device:"

[link to en.wikipedia.org]

Could you also help me understand: what do suppose it means on p 503 " medical device surveillance?"

Call me paranoid, but I'd like to know what is going on.... I'd feel more comfortable second guessing these things before the fact....rather than after. These are serious red flags that we need to pay careful attention to...imo.
The White House (OP)
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11/20/2009 02:21 PM
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TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER H--MEDICAL DEVICES
PART 880 -- GENERAL HOSPITAL AND PERSONAL USE DEVICES
Sec. 880.6300 Implantable radiofrequency transponder system for patient identification and health information.
And if you have a public health system then you naturally need to register the patients to eliminate abuse of the system.
Anonymous Coward
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11/20/2009 02:22 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
Don't freak everyone.

They know damn well this will not possibly fly.

too many of us .. too few of them.

Like the vaccines though, many sheep will go willingly and some will try to push to the front of the line.
Anonymous Coward
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11/20/2009 02:22 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
Implantable Radiofrequency Transponder System for Patient Identification and Health Information
Anonymous Coward
11/20/2009 02:24 PM
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And the shills come along with their BS flags!!!


muaha


That's when you know for sure that a post is important.
Anonymous Coward
User ID: 804173
United States
11/20/2009 02:25 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
Don't freak everyone.

They know damn well this will not possibly fly.

too many of us .. too few of them.

Like the vaccines though, many sheep will go willingly and some will try to push to the front of the line.
 Quoting: Anonymous Coward 821753


This will be apart of the healthcare system, it will fly in most minds of the populace because of how hard they've been coerced into the "healthcare at all costs" mindset. This is where the all costs comes into play.
JDUB
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11/20/2009 02:25 PM
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OP is right. the World will be forced to take the implant. With daily increasing rate of illnesses and terrorism we'll be seeing this becoming more and more popular over the next few years.
Anonymous Coward
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11/20/2009 02:26 PM
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And the shills come along with their BS flags!!!


muaha


That's when you know for sure that a post is important.
 Quoting: Mister Obvious


Absolutely right. You know they don't have a leg to stand on when they can only hurl personal attacks.
The White House (OP)
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11/20/2009 02:26 PM
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sd1975

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11/20/2009 02:27 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
Jack be nimble,

Jack be quick.

"What the Fuck's up with this micro-chip?"

Subtitle C-11 Sec. 2521 National Medical Device Registry

"... 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 that has been used in or on a patient; and (B) is a Class III device; or (ii) A Class II device that is Implantable..."
[link to www.rense.com]
 Quoting: The White House 799732



I always predicted that Health Care will be a big part of the implementation of the mark of the beast system during the tribulation period. I connected the two a long time ago...can't prove it and I don't care...but outbreak will be a big part...healthcare/disease/pestilence then tie the entire healthcare system into the financial system and finally the implementation of 'The Mark' (Which in part will be tied into everything financial).
'This is the strangest life I've ever known'...James Douglas Morrison
Anonymous Coward
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11/20/2009 02:28 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
I'm already working on hacking the RF chip. Should be easy enough. A combo of RF remote hacks and wifi encription should be all that is needed. I'm just hoping there is SSNs in the chip... Easy as pie...
 Quoting: Anonymous Coward 822841



Whatever you find out, or if anyone can find out WHO is making the thing, please post on GLP. I'd like to know if I'm working for the wrong company.
Hitndahedfred
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11/20/2009 02:28 PM
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[link to edocket.access.gpo.gov]

Appears legit to me
Hitndahedfred
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11/20/2009 02:30 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
§ 880.6300 21 CFR Ch. I (4–1–06 Edition)
(b) Classification. Class I (general controls).
The device is exempt from the
premarket notification procedures in
subpart E of part 807 of this chapter,
subject to the limitations in § 880.9.
[45 FR 69682–69737, Oct. 21, 1980, as amended
at 54 FR 25050, June 12, 1989; 66 FR 38806, July
25, 2001]
§ 880.6300 Implantable radiofrequency
transponder system for patient
identification and health information.
(a) Identification. An implantable radiofrequency
transponder system for
patient identification and health information
is a device intended to enable
access to secure patient identification
and corresponding health information.
This system may include a passive implanted
transponder, inserter, and
scanner. The implanted transponder is
used only to store a unique electronic
identification code that is read by the
scanner. The identification code is used
to access patient identity and corresponding
health information stored
in a database.
(b) Classification. Class II (special
controls). The special control is FDA’s
guidance document entitled ‘‘Class II
Special Controls Guidance Document:
Implantable Radiofrequency Transponder
System for Patient Identification
and Health Information.’’ See
§ 880.1(e) for the availability of this
guidance document. This device is exempt
from the premarket notification
procedures in subpart E of part 807 of
this chapter subject to the limitations
in § 880.9.
[69 FR 71704, Dec. 10, 2004]
§ 880.6320 AC-powered medical examination
light.
(a) Identification. An AC-powered
medical examination light is an ACpowered
device intended for medical
purposes that is used to illuminate
body surfaces and cavities during a
medical examination.
(b) Classification. Class I (general controls).
The device is exempt from the
premarket notification procedures in
subpart E of part 807 of this chapter,
subject to the limitations in § 880.9.
[45 FR 69682–69737, Oct. 21, 1980, as amended
at 61 FR 1123, Jan. 16, 1996; 66 FR 38806, July
25, 2001]
§ 880.6350 Battery-powered medical
examination light.
(a) Identification. A battery-powered
medical examination light is a batterypowered
device intended for medical
purposes that is used to illuminate
body surfaces and cavities during a
medical examination.
(b) Classification. Class I (general controls).
The device is exempt from the
premarket notification procedures in
subpart E of part 807 of this chapter,
subject to the limitations in § 880.9. The
device also is exempt from the current
good manufacturing practice regulations
in part 820 of this chapter, with
the exception of § 820.180, with respect
to general requirements concerning
records, and § 820.198, with respect to
complaint files.
[45 FR 69682–69737, Oct. 21, 1980, as amended
at 66 FR 38806, July 25, 2001]
§ 880.6375 Patient lubricant.
(a) Identification. A patient lubricant
is a device intended for medical purposes
that is used to lubricate a body
orifice to facilitate entry of a diagnostic
or therapeutic device.
(b) Classification. Class I (general controls).
[45 FR 69682–69737, Oct. 21, 1980, as amended
at 66 FR 46952, Sept. 10, 2001]
§ 880.6430 Liquid medication dispenser.
(a) Identification. A Liquid medication
dispenser is a device intended for
medical purposes that is used to issue a
measured amount of liquid medication.
(b) Classification. Class I (general controls).
The device is exempt from the
premarket notification procedures in
subpart E of part 807 of this chapter,
subject to the limitations in § 880.9. The
device is also exempt from the current
good manufacturing practice regulations
in part 820 of this chapter, with
the exception of § 820.180, with respect
to general requirements concerning
records, and § 820.198, with respect to
complaint files.
[45 FR 69682–69737, Oct. 21, 1980, as amended
at 66 FR 38806, July 25, 2001]
§ 880.6450 Skin pressure protectors.
(a) Identification. A skin pressure protector
is a device intended for medical
VerDate Aug<
The White House (OP)
User ID: 799732
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11/20/2009 02:33 PM
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Connecting the Dots: Exposing RFID Documents and Plans For Surveilling
[link to preventdisease.com]

Radio Frequency Implantable Device (RFID) use on humans can no longer be claimed as speculation or theory. Their use is now well documented and integrated in several planned strategies for the U.S. Department of Health and Human Services and Health Care Bills. These disturbing initiatives will see microchip implants embedded inside every American, and possibly inside every human within the next few years.

Richard Schmid has worked in radiological health for more than a decade. He has been researching RFID chips for most of his professional career and has worked extensively with RF devices in all levels of radiological medicine. He admits that his analysis of U.S. Health Care Bills and RFID documentation is alarming. "I don't think most people understand the magnitude of what is happening with the health care legislation being imposed on Americans," he stated.

Schmid says that RFID chips have already been implanted in thousands of people around the world, many without their knowledge. "Some of these devices are so small and scalable, that they are capable of being inserted in food, patches, medications, hypodermic needles and even inside vaccines." A recent report from PreventDisease.com detailed how populations are being primed for nano-microchips inside vaccines.

"I used to joke with colleagues about pandemic scenarios and airborne plagues and how that would be the only way for people to submit to implantable chips....I just never thought it would come true in the exact scenario I had imagined." Schmid said that the current situation in the Ukraine and media blackout in the west are a bad sign of things to come.

As the World Health Organization (WHO) continues to deceive the world on the current pandemic affecting the Ukraine and surrounding area, many experts well-versed in the WHO's manipulation are calling the current reporting of Ukraine's pandemic as one of the most deceptive in the agency's history. Not only is the WHO refusing to release the actual number of deaths, but they also continue to delay the release of critical sequencing data for the mutated strain. The illness has infected well over one million people in the Ukraine and has spread to neighboring countries with similar infection rates. The actual number of deaths are rumoured to be much higher than those reported by the Ukraine government and the WHO.

Schmid said that the pandemic will be a ploy to begin implanting the RFIDs in millions of people in the United States. "We're likely just weeks away from this Ukraine plague hitting the U.S. They haven't halted air travel, transport or made any attempts to advise the American people." He speculated that the pandemic would be the trigger to start incrementally phasing in the devices until they become mandatory.

Schmid added that people who initially refuse the device will not be able to obtain or renew essential documents like passports, driver's licenses, med cards, and all credit/banking cards. "It's a totally new electronic system, but they've been developing it for years and it will soon be integrated with all National ID cards around the world." Schmid says the public will not be able to get back on to the grid without the RFID, something that will eventually be required from every nation.
The White House (OP)
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11/20/2009 02:35 PM
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WHO is making the thing, please post on GLP. I'd like to know if I'm working for the wrong company.
 Quoting: Anonymous Coward 805464


Hitachi Develops a New RFID with Embedded Antenna µ-Chip

--Makes Possible Wireless Links that Work Using Nothing More Than a 0.4mm X 0.4mm Chip, One of the World's Smallest ICs--

[link to www.hitachi.com]
The White House (OP)
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11/20/2009 02:39 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
In December 10, 2004, a document was released by the U.S. Department of Health and Human Services that detailed special controls guidance for radio frequency transponders of patient identification. The document details everything from the performance testing to the electromagnetic and resonance imaging capabilities of the device. The FDA cleared VeriChip for medical applications in the U.S. two months before the document was released.

VeriChip is the first Food and Drug Administration (FDA)-approved human-implantable radio-frequency identification (RFID) microchip. About twice the length of a grain of rice, the device is typically implanted above the triceps area of an individual’s right arm. Once scanned at the proper frequency, the VeriChip responds with a unique 16 digit number which could be then linked with information about the user held on a database for identity verification, medical records access, and used for identification by a third party.

In May 2005, the U.S. Congress passed the "Real ID" Act, which required states to issue federally approved driver's licenses or identification (ID) cards to those who live and work in the United States. The identity cards will eventually be integrated with the RFID chips if one wants to drive, visit a federal government building, collect Social Security, access a federal government service or use the services of a private entity (such as a bank or an airline) that is required under federal law to verify customer identity. The goal is to make it nearly impossible to live without such an ID.
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11/20/2009 02:39 PM
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Re: Unbelievable!!! Health Care Bill Mandates Implantable Micro-Chip!
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