OBAMA CARE BILL- implantable devise, Class II device; will it happen on 23 March 2013?
*Obama Care, will the Law to implant micro chips be strictly enacted on 23 March 2013?
*This is the question running through the minds of most of the Americans and some other who expect the Beast system to be imposed.
*We all know the News running through the end time signs tracking sites.
*First of all I would like to say that I am not standing on any ones side, by doing this.
Let us Examine those US bills which deal with this subject:
The first bill is HR: 3200.-America’s Affordable Health Choices Act of 2009 (or HR 3200).
The proposed America’s Affordable Health Choices Act of 2009 (or HR 3200)[1] was an unsuccessful bill introduced in the U.S. House of Representativeson July 14, 2009. but was superseded by a similar bill, the proposed Affordable Health Care for America Act (HR 3962), which was passed by the House in November 2009, by a margin of 220-215 votes.
Source: http://en.wikipedia.org/wiki/America’s_Affordable_Health_Choices_Act_of_2009
So now let’s examine HR 3962
The Affordable Health Care for America Act (or HR 3962)[1] was a bill that was crafted by the United States House of Representatives in November 2009. This bill was passed in the House, , but the Affordable Health Care for America Act as originally drafted never became law. On December 24, 2009, the Senate passed an alternative health care bill, the Patient Protection and Affordable Care Act (H.R. 3590).[2] In 2010, the House abandoned its reform bill in favor of amending the Senate bill (via the reconciliation process) in the form of the Health Care and Education Reconciliation Act of 2010. A different bill, under the same bill number H.R. 3962, was eventually passed by Congress and, on June 25, 2010, was signed by the President. This is the “Preservation of Access to Care for Medicare Beneficiaries and Pension Relief Act of 2010.”
source:http://en.wikipedia.org/wiki/Affordable_Health_Care_for_America_Act#H.R._3962_as_eventually_enacted
So now let’s examine HR 3590
The Patient Protection and Affordable Care Act (PPACA),[1] commonly called Obamacare[2][3] or the Affordable Care Act, is a United Statesfederal statute signed into law by President Barack Obama on March 23, 2010. Together with the Health Care and Education Reconciliation Act,it represents the most significant government expansion and regulatory overhaul of the U.S. healthcare system since the passage of Medicare andMedicaid in 1965.
There are 7 versions of Bill Number H.R.3590 for the 111th Congress. Usually, the last item is the most recent:
Patient Protection and Affordable Care Act (Enrolled Bill [Final as Passed Both House and Senate]
Dec 2009 public print.
SEC. 9009. IMPOSITION OF ANNUAL FEE ON MEDICAL DEVICE MANUFACTURERS AND IMPORTERS.
Page 745 & 746
(d) MEDICAL DEVICE SALES.—For purposes of this section—(1) IN GENERAL.—The term ‘‘medical device sales’’ means sales for use in the United States of any medical device, other than the sales of a medical device that—
(A) has been classified in class II under section 513 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C.360c) and is primarily sold to consumers at retail for not more than $100 per unit, or
(3) MEDICAL DEVICE.—For purposes of paragraph (1), the term ‘‘medical device’’ means any device (as defined in section 201(h) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321(h))) intended for humans.
So this bill only talks about medical device sales. But in this section we can see mentioning about the sale of a class II device which corresponds to section 513 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C.360c).
This is a definition by FDA of class II device: `(ii) a class II device which is intended to be permanently implantable or life sustaining or life supporting; or ``(1) implanted in the human body for more than one year, or (2) a life sustaining or life supporting device used outside a device user facility. (this could be any thing like pace maker, breast implant, etc).
ODE Guidance 1998 – 2009
So now let’s examine HR 4872
The Health Care and Education Reconciliation Act of 2010 (Pub.L. 111–152, 124 Stat. 1029) is a law that was enacted by the 111th United States Congress, by means of the reconciliation process, in order to amend the Patient Protection and Affordable Care Act (Pub.L. 111–148). It was signed into law by President Barack Obama on March 30, 2010.
Obama signed the Patient Protection and Affordable Care Act into law on March 23, 2010. The Health Care and Education Reconciliation Act of 2010 was passed by the House of Representatives on March 21, 2010, by a vote of 220–211, and on March 25, after having two minor provisions stricken under the Byrd Rule, passed the Senate by a vote of 56-43. A few hours later, the amended bill was passed by the House 220-207. President Obama signed the health care reconciliation bill into law on Tuesday, March 30, at Northern Virginia Community College.
March 17. 2010. H.R.4872 — Reconciliation Act of 2010 (Reported in House – RH) in the house of representatieves and passed on 21 Mar 2010.
following is a part from that bill:
Title V—Other provisions-
Subtitle C–National Medical Device Registry
SEC. 2521. NATIONAL MEDICAL DEVICE REGISTRY. (source)
(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 subsection (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.
H.R.4872 — Resolved, That the bill from the House of Representatives (H.R. 4872) entitled `An Act to provide for reconciliation
pursuant to Title II of the concurrent resolution on the budget… (Engrossed Amendment Senate – EAS)
‑HR 4872 EAS In the Senate of the United States,March 25, 2010.
Resolved, That the bill from the House of Representatives (H.R. 4872) entitled `An Act to provide for reconciliation pursuant to Title II of the concurrent
resolution on the budget for fiscal year 2010 (S. Con. Res. 13).’, do pass with the following AMENDMENTS:
( 1 ) On page 118, strike lines 15 through 25 (and redesignate subsequent subsections accordingly).
( 2 ) On page 120, strike lines 3 through 5.
Attest: Secretary.111th CONGRESS 2d Session H.R. 4872 AMENDMENTS
H.R.4872 — Health Care and Education Reconciliation Act of 2010
(Enrolled Bill [Final as Passed Both House and Senate] – ENR)
But in this last(Mar 30) passed version I dont see the above mentioned part, instead only this that talks about medical devices:
1405. Excise tax on medical device manufacturers.
(a) IN GENERAL.—Chapter 32 of the Internal Revenue Code of 1986 is amended—
(1) by inserting after subchapter D the following new subchapter:
Subchapter E—Medical Devices
‘‘Sec. 4191. Medical devices. ‘‘SEC. 4191. MEDICAL DEVICES.
‘‘(a) IN GENERAL.—There is hereby imposed on the sale of any taxable medical device
by the manufacturer, producer, or importer a tax equal to 2.3 percent of the price for
which so sold.‘‘(b) TAXABLE MEDICAL DEVICE.—For purposes of this section
‘‘(1) IN GENERAL.—The term ‘taxable medical device’ means any device
(as defined in section 201(h) of the Federal Food, Drug, and Cosmetic Act) intended
for humans. ‘‘(2) EXEMPTIONS.—Such term shall not include—Definition. 26 USC 4191.
I dont know why this is so…!!!!
Conclusion:
So by now we know that bill no. HR 3590 and HR 4872 were the Health care bills signed by OBAMA. And in both of the final Version of the bills there are no clear mentioning of the term Implantable device rather only talks about the sale and taxing “Class II device”. The funny thing is that Implantable devices come under “Class II devices/Medical device”. And the FDA has interesting definition for this.
(Guidance for Industry and FDA Staff – Class II Special Controls Guidance Document: Implantable Radiofrequency Transponder
System for Patient Identification and Health Information.)
In HR 3962 I have seen this portion:
“(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. “
This could be the reason why people say “IT WILL HAPPEN ON 23 MARCH 2013”.
But for me, as I said I am on nobodies side, neither with those say RFID in Obama care is a hoax nor with those say Obama care is talking about RFID.
Because I don’t know..!! and this is only an assessment. If any thing mentioned above regarding the bills are not correct please kindly leave a message..!!!
Sources : Wikipedia and http://thomas.loc.gov/home/thomas.php
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above mentioned opinion is mine only and nothing to do with the below given site:
For signs of time: www.emperoremmanuel.com
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Whistler Blowers, Insiders
I think chipping Americans is a brilliant idea. That way Britain will be able to spot and charge all the American health tourists stealing from the British tax payer.
Pure genius.