[Rushtalk] Micro-chipping Humans Is On The Way!

John A. Quayle blueoval57 at verizon.net
Sat Feb 16 20:04:07 MST 2013


At 09:59 PM 2/15/2013, Paf Dvorak wrote:
>At 09:46 PM 2/15/2013 -0500, John A. Quayle wrote:
>>
>>         H.R. 3200 of 2009 had language about 
>> the RFID chip but was not passed into law. The 
>> language for that was removed in HR 3590. This 
>> is not an issue as far as Obamacare goes but 
>> it sure is on the table and as we both know, 
>> it is just a matter of time till the fit it 
>> into another bill to get it through.
>
>That's what I said.

         Not exactly...........






>>At 04:32 PM 2/15/2013, Paf Dvorak wrote:
>>>At 11:52 PM 2/14/2013 -0800, Tom Matiska wrote:
>>>>Snopes says false... but it is an interesting read....
>>>>
>>>> 
>>>><http://www.snopes.com/politics/medical/microchip.asp>http://www.snopes.com/politics/medical/microchip.asp
>>>>
>>>>To summarize for the research impaired: no 
>>>>such language was in the final bill..... but 
>>>>initial and reconciliation versions of HR 
>>>>4872 came close.... but that language didn't 
>>>>require the chip, but allowed for a registry 
>>>>to be created for the purpose of tracking 
>>>>implants such as pacemakers and hip 
>>>>replacements (hmmm.... is there an implant 
>>>>show loophole that allows unregistered 
>>>>sales???).... the micro implant shown in many 
>>>>version of this story is actually a glucose 
>>>>measuring device(which any good conspiracy 
>>>>buff will tell you is just the cover story to conceal its true purpose)
>>>>
>>>>Tom
>>>
>>>Oh well...Snopes! Everyone knows Snopes is 
>>>part of the Vast Liberal Conspiracy® designed 
>>>to trick We The People into believing stuff that's not true and vice versa.
>>>Anyway, here's the 
>>><http://housedocs.house.gov/energycommerce/ppacacon.pdf>Final 
>>>Version. (It's a .pdf) For the software 
>>>impaired, once the pdf is open, (on a windoze 
>>>PC) hold down the Ctrl key and hit the f, then type in some search terms.
>>>
>>>Follows the stuff they took out if the final bill:
>>>What is telling though, and something we 
>>>should all be aware of: The stuff they took 
>>>out was originally in there! They still want 
>>>to chip us and other crap to give them power 
>>>over us! And if you're over the age of 50 
>>>you've likely seen tyrannical incrementalism 
>>>used on us already. It's what they;ve been 
>>>doing and are doing again with guns. They've 
>>>been chipping away at ALL of our liberties 
>>>since the nation was founded! They even did it 
>>>when they created the present constitution! 
>>>They were just gonna go and tweak it a little 
>>>bit...iron out some wrinkles they missed the 
>>>first time. Our foretyrants didn't go planning 
>>>on having a constitutional convention, they 
>>>forced one on the nation. They will do as much as we allow them to do.
>>>Thanks John for being vigilant.
>>>
>>>
>>>
>>>
>>>
>>>Subtitle C­National Medical Device Registry
>>>SEC. 2521. NATIONAL MEDICAL DEVICE REGISTRY.
>>>(a) REGISTRY.­
>>>
>>>
>>>
>>>
>>>
>>>
>>>
>>>(1) IN GENERAL.­Section 519 of the Federal 
>>>Food, Drug, and Cosmetic Act (21 U.S.C. 360i) is amended­
>>>(A) by redesignating subsection (g) as sub5 section (h); and
>>>(B) by inserting after subsection (f) the following:
>>>‘‘National Medical Device Registry” (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; 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 Coordinator 
>>>for Health Information Technology, and the 
>>>Secretary of Veterans Affairs, determine the best methods for­
>>>(A) 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;
>>>(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), including, 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 section 
>>>505(k) (relating to active postmarket risk 
>>>identification); (ii) activities under 
>>>paragraph (4) of section 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 (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 Coordinator for 
>>>Health Information Technology, and the 
>>>Secretary of Veterans Affairs, determine the 
>>>best methods for­(A) 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; (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), 
>>>including, 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 section 505(k) (relating to active 
>>>postmarket risk identification); (ii) 
>>>activities under paragraph (4) of section 
>>>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, 
>>>academic, 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 program under title XVIII of the 
>>>Social Security 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 assessment 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 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.
>>>
>>>(4) Not later than 36 months after the date of 
>>>the enactment of this subsection, the 
>>>Secretary shall promulgate regulations for 
>>>establishment and operation of the registry under paragraph (1).
>>>
>>>(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 manufacturers of 
>>>such devices to submit information to the 
>>>registry, including, for each such device, the 
>>>type, model, and serial number or, if required 
>>>under subsection (f), other unique device 
>>>identifier; and (ii) in the case of devices 
>>>that are described in paragraph (1) and sold 
>>>before such date, may require 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 submitted pursuant to 
>>>subparagraph (A) with patient safety and 
>>>outcomes data obtained under paragraph (3); 
>>>and (ii) to permit analyses of linked data;
>>>(C) may require device manufacturers to submit 
>>>such other information as is necessary to 
>>>facilitate postmarket assessments of device 
>>>safety and effectiveness 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 prevalence 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 proprietary information 
>>>and is comprehensive, useful, and not 
>>>misleading to patients, physicians, and scientists.
>>>(5) To carry out this subsection, there are 
>>>authorized 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 enactment 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 amended 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 
>>>National Coordinator for Health Information 
>>>Technology 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 
>>>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), if 
>>>such an identifier is required by section 
>>>519(f) of the Federal Food, Drug, and Cosmetic 
>>>Act U.S.C. 360i(f)) for the device.
>>>
>>>In its final version ­ the actual 974-page 
>>>Obamacare law ­ even that “National Medical 
>>>Device Registry” section is deleted.
>>>
>>>In re incrementalism and the constitution:
>>>
>>>Lest we've not brushed up on history in some time,
>>>
>>>"The Constitutional Convention (also known as 
>>>the Philadelphia Convention, the Federal 
>>>Convention, or the Grand Convention at 
>>>Philadelphia) took place from May 25 to 
>>>September 17, 1787, in Philadelphia, 
>>>Pennsylvania, to address problems in governing 
>>>the United States of America, which had been 
>>>operating under the Articles of Confederation 
>>>following independence from Great Britain. 
>>>Although the Convention was intended to revise 
>>>the Articles of Confederation, the intention 
>>>from the outset of many of its proponents, 
>>>chief among them James Madison and Alexander 
>>>Hamilton, was to create a new government 
>>>rather than fix the existing one. The 
>>>delegates elected George Washington to preside 
>>>over the Convention. The result of the 
>>>Convention was the United States Constitution, 
>>>placing the Convention among the most 
>>>significant events in the history of the United States."
>>>
>>>Kinda makes that most important document seem 
>>>like something of a whim, and just as binding.
>>>
>>>http://en.wikipedia.org/wiki/Constitutional_Convention_%28United_States%29
>>>
>>>
>>>>
>>>>
>>>>- On Thu, 2/14/13, John A. Quayle <blueoval57 at verizon.net> wrote:
>>>>From: John A. Quayle <blueoval57 at verizon.net>
>>>>Subject: [Rushtalk] Micro-chipping Humans Is On The Way!
>>>>To: "Rushtalk" <rushtalk at csdco.com>
>>>>Date: Thursday, February 14, 2013, 10:42 PM
>>>>
>>>>
>>>>
>>>>
>>>>
>>>>
>>>>Micro Chip Implant Coming March 23, 2013
>>>>The New Health Care (Obama care) law H.R. 
>>>>3590 Also HR 4872 requires all US citizens to have the RFID implanted
>>>>SHARE THIS WITH EVERYONE YOU KNOW, GET THE WORD OUT !
>>>>This evil plan is being launched by America. 
>>>>its a micro chip injected in your hand. it 
>>>>will contain all your personal data heath and 
>>>>bank accounts etc. its also a GPS device 
>>>>being monitored. they can deactivate it at 
>>>>any time if they find you suspicious or not 
>>>>loyal to their government or go against them 
>>>>or their system and you will lose everything 
>>>>you ever had. soon this device will be made 
>>>>common just like they did credit cards, 
>>>>turning paper money into digital money. means 
>>>>nothing is physically in your hand. it will 
>>>>be made a must for every citizen with time 
>>>>according to their plan and then they will 
>>>>spread it outside America so they can monitor 
>>>>and control as many people as they can and 
>>>>turn them into slaves with their digital technologies.
>>>>this device is the future or slavery
>>>>BEWARE of this EVIL DEVICE. if you don't 
>>>>believe me do your own research before you come to argue or debate.
>>>>
>>>>
>>>>
>>>>
>>>>
>>>>
>>>>
>>>>
>>>>
>>>>[]
>>>>
>>>>
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>>>>
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>>>
>>>Paf Dvorak
>>>
>>><http://thatswaytoomuch.info/>notmyname at thatswaytoomuch.info
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>
>Paf Dvorak
>
><http://thatswaytoomuch.info/>notmyname at thatswaytoomuch.info
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