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Have You Already Been "Chipped"?

Updated on June 4, 2015

Have you been to the Doctor lately? Possibly the hospital?

I sure hate breaking this to you, but there is a very good possibility you have one of these devices implanted in you.

I can hear and see many of you right now; there goes Froggy and his conspiracies again while you are rolling your eyes. Before you jump to that conclusion, let me give you sound reasoning. If you can show me a good reason not to believe this, I will listen!

I want to thank my friend Dan who has kept me aware of this and opened my eyes. His site is linked below.

Health Care Bill

Ok, here's the proof.

The Health-Care bill passed right?

You will find below this chapter the link to the entire bill in P.D.F. format.

What is being quoted here is section 1001 which absolutely states that any and all medical patients will receive an implanted device and I read nowhere in this bill where the patient even has to be asked or even told they are getting one. If you read it differently, please tell me. I don't see it. Here is what I have read:

9 Subtitle C—National Medical
10 Device Registry
12 (a) REGISTRY.—
13 (1) IN GENERAL.—Section 519 of the Federal
14 Food, Drug, and Cosmetic Act (21 U.S.C. 360i) is
15 amended—
16 (A) by redesignating subsection (g) as sub17
section (h); and
18 (B) by inserting after subsection (f) the
19 following:
20 ‘‘National Medical Device Registry
21 ‘‘(g)(1) The Secretary shall establish a national med22
ical device registry (in this subsection referred to as the
23 ‘registry’) to facilitate analysis of postmarket safety and
24 outcomes data on each device that—
25 ‘‘(A) is or has been used in or on a patient; and
VerDate Nov 24 2008 12:51 Jul 14, 2009 Jkt 000000 PO 00000 Frm 01001 Fmt 6652 Sfmt 6201 C:\TEMP\AAHCA0~1.XML HOLCPC
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1 ‘‘(B) is—
2 ‘‘(i) a class III device; or
3 ‘‘(ii) a class II device that is implantable,
4 life-supporting, or life-sustaining.
5 ‘‘(2) In developing the registry, the Secretary shall,
6 in consultation with the Commissioner of Food and Drugs,
7 the Administrator of the Centers for Medicare & Medicaid
8 Services, the head of the Office of the National Coordi9
nator for Health Information Technology, and the Sec10
retary of Veterans Affairs, determine the best methods
11 for—
12 ‘‘(A) including in the registry, in a manner con13
sistent with subsection (f), appropriate information
14 to identify each device described in paragraph (1) by
15 type, model, and serial number or other unique iden16
17 ‘‘(B) validating methods for analyzing patient
18 safety and outcomes data from multiple sources and
19 for linking such data with the information included
20 in the registry as described in subparagraph (A), in21
cluding, to the extent feasible, use of—
22 ‘‘(i) data provided to the Secretary under
23 other provisions of this chapter; and
24 ‘‘(ii) information from public and private
25 sources identified under paragraph (3);
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July 14, 2009 (12:51 p.m.)
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1 ‘‘(C) integrating the activities described in this
2 subsection with—
3 ‘‘(i) activities under paragraph (3) of sec4
tion 505(k) (relating to active postmarket risk
5 identification);
6 ‘‘(ii) activities under paragraph (4) of sec7
tion 505(k) (relating to advanced analysis of
8 drug safety data); and
9 ‘‘(iii) other postmarket device surveillance
10 activities of the Secretary authorized by this
11 chapter; and
12 ‘‘(D) providing public access to the data and
13 analysis collected or developed through the registry
14 in a manner and form that protects patient privacy
15 and proprietary information and is comprehensive,
16 useful, and not misleading to patients, physicians,
17 and scientists.
18 ‘‘(3)(A) To facilitate analyses of postmarket safety
19 and patient outcomes for devices described in paragraph
20 (1), the Secretary shall, in collaboration with public, aca21
demic, and private entities, develop methods to—
22 ‘‘(i) obtain access to disparate sources of
23 patient safety and outcomes data, including—
24 ‘‘(I) Federal health-related electronic
25 data (such as data from the Medicare pro-
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July 14, 2009 (12:51 p.m.)
f:\VHLC\071409\071409.140.xml (444390|2)
1 gram under title XVIII of the Social Secu2
rity Act or from the health systems of the
3 Department of Veterans Affairs);
4 ‘‘(II) private sector health-related
5 electronic data (such as pharmaceutical
6 purchase data and health insurance claims
7 data); and
8 ‘‘(III) other data as the Secretary
9 deems necessary to permit postmarket as10
sessment of device safety and effectiveness;
11 and
12 ‘‘(ii) link data obtained under clause (i)
13 with information in the registry.
14 ‘‘(B) In this paragraph, the term ‘data’ refers to in15
formation respecting a device described in paragraph (1),
16 including claims data, patient survey data, standardized
17 analytic files that allow for the pooling and analysis of
18 data from disparate data environments, electronic health
19 records, and any other data deemed appropriate by the
20 Secretary.
21 ‘‘(4) Not later than 36 months after the date of the
22 enactment of this subsection, the Secretary shall promul23
gate regulations for establishment and operation of the
24 registry under paragraph (1). Such regulations—
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1 ‘‘(A)(i) in the case of devices that are described
2 in paragraph (1) and sold on or after the date of the
3 enactment of this subsection, shall require manufac4
turers of such devices to submit information to the
5 registry, including, for each such device, the type,
6 model, and serial number or, if required under sub7
section (f), other unique device identifier; and
8 ‘‘(ii) in the case of devices that are described in
9 paragraph (1) and sold before such date, may re10
quire manufacturers of such devices to submit such
11 information to the registry, if deemed necessary by
12 the Secretary to protect the public health;
13 ‘‘(B) shall establish procedures—
14 ‘‘(i) to permit linkage of information sub15
mitted pursuant to subparagraph (A) with pa16
tient safety and outcomes data obtained under
17 paragraph (3); and
18 ‘‘(ii) to permit analyses of linked data;
19 ‘‘(C) may require device manufacturers to sub20
mit such other information as is necessary to facili21
tate postmarket assessments of device safety and ef22
fectiveness and notification of device risks;
23 ‘‘(D) shall establish requirements for regular
24 and timely reports to the Secretary, which shall be
25 included in the registry, concerning adverse event
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July 14, 2009 (12:51 p.m.)
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1 trends, adverse event patterns, incidence and preva2
lence of adverse events, and other information the
3 Secretary determines appropriate, which may include
4 data on comparative safety and outcomes trends;
5 and
6 ‘‘(E) shall establish procedures to permit public
7 access to the information in the registry in a manner
8 and form that protects patient privacy and propri9
etary information and is comprehensive, useful, and
10 not misleading to patients, physicians, and sci11
12 ‘‘(5) To carry out this subsection, there are author13
ized to be appropriated such sums as may be necessary
14 for fiscal years 2010 and 2011.’’.
15 (2) EFFECTIVE DATE.—The Secretary of
16 Health and Human Services shall establish and
17 begin implementation of the registry under section
18 519(g) of the Federal Food, Drug, and Cosmetic
19 Act, as added by paragraph (1), by not later than
20 the date that is 36 months after the date of the en21
actment of this Act, without regard to whether or
22 not final regulations to establish and operate the
23 registry have been promulgated by such date.
25 303(f)(1)(B)(ii) of the Federal Food, Drug, and
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July 14, 2009 (12:51 p.m.)
f:\VHLC\071409\071409.140.xml (444390|2)
1 Cosmetic Act (21 U.S.C. 333(f)(1)(B)(ii)) is amend2
ed by striking ‘‘519(g)’’ and inserting ‘‘519(h)’’.
7 Committee established under section 3002 of the
8 Public Health Service Act (42 U.S.C. 300jj–12)
9 shall recommend to the head of the Office of the Na10
tional Coordinator for Health Information Tech11
nology standards, implementation specifications, and
12 certification criteria for the electronic exchange and
13 use in certified electronic health records of a unique
14 device identifier for each device described in section
15 519(g)(1) of the Federal Food, Drug, and Cosmetic
16 Act, as added by subsection (a).
19 the Health Human Services, acting through the
20 head of the Office of the National Coordinator for
21 Health Information Technology, shall adopt stand22
ards, implementation specifications, and certification
23 criteria for the electronic exchange and use in cer24
tified electronic health records of a unique device
25 identifier for each device described in paragraph (1),

I do know what I pasted here is very hard to read--so to read it yourself out of the actual health-care bill follow the link and start at section 1001.


Ok, lets hear it.

I know that some attacks will come because many people are apathetic and just want everything to go "smooth". Well life isn't smooth and "chipping" people will happen because "we the people" allowed it.

Here are some other links to open your mind:

Will They?

Do You Think You Will Be "Chipped"

See results

© 2010 Greg Boudonck


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    • Froggy213 profile image

      Greg Boudonck 6 years ago from Returned to an Isla Del Sol - Puerto Rico Will Rise Strong

      Really no way of knowing, but any foreign object in your body will not want to stay there. Itching and discomfort will be a sign.

    • profile image

      MARIA 6 years ago


    • Froggy213 profile image

      Greg Boudonck 7 years ago from Returned to an Isla Del Sol - Puerto Rico Will Rise Strong

      Thanks for reading Harlan--you have me lol with this comment!!

    • Harlan Colt profile image

      Harlan Colt 7 years ago from the Rocky Mountains

      They don't want to try to chip me so as I know about it.

      Here is the conversation from the health worker when they get home.

      "Hard day at work today dear?"

      "Yea some hill-billy blacked my eye when I tried to chip him, and then shoved the syringe up my rear."

      - Best wishes

      - Harlan

    • Entourage_007 profile image

      Stuart 7 years ago from Santa Barbara, CA

      if you got an MRI (Magnetic Resonance Imaging) this would likely show up because it is largely involved with using magnets. At least that would find it, but I don't know if it would disable it.

      There needs to be action taken on this stupid act that allows this. The point is - no one wants a chip inside their body.

    • profile image

      st@r 7 years ago

      yes how u no if u were chipped

    • profile image

      vidal 7 years ago

      how would you know if u were chipped ?

    • profile image

      CollB 7 years ago

      Interesting article. I haven't been chipped yet as I've not had any operations for a long while. Now I'll just be more aware when I go to the doctors.

    • profile image

      fooch 7 years ago

      Google hitachi powder type RFID. They are making RFID's smaller and smaller. I'm sure they already have it ready.

      I wouldn't even get my pet chipped.

    • profile image

      judy 7 years ago

      stop the madness people- do u think they can slip that into you.while u r worried about this, something else that's real is happenning.

    • QudsiaP1 profile image

      QudsiaP1 7 years ago

      Fascinating and terrifying.

    • profile image

      SirDent 7 years ago

      Rev 13:16 And he causeth all, both small and great, rich and poor, free and bond, to receive a mark in their right hand, or in their foreheads:

      Rev 13:17 And that no man might buy or sell, save he that had the mark, or the name of the beast, or the number of his name.

      Rev 13:18 Here is wisdom. Let him that hath understanding count the number of the beast: for it is the number of a man; and his number is Six hundred threescore and six.

      Thanks for bringing this to the attention of those who want to know.

    • electricsky profile image

      electricsky 7 years ago from North Georgia

      They did this to my dog and the Manchurian candidate, but I really do not want one on myself.

      Thanks for the article.

    • ptosis profile image

      ptosis 7 years ago from Arizona

      In the x-files they put it up deep into Scully's nose. I though behind the ear ( like pets ) would be the place. It would have to be someplace that I could not get my hands on because I would just cut it out.

      Ohh -oh - I just thought of a place - I had a colonoscopy a decade ago ... no .. no! ....NOOOOO!

    • profile image

      Deuce 7 years ago

      The fuck? are you affiliated with FOX news? All you're doing is spreading fear.

    • bonnebartron profile image

      bonnebartron 7 years ago from never one place for too long

      All I have to say is WTF!? Excuse me everyone... I have research to do!

    • profile image

      Robert 8 years ago

      It's pretty easy to figure out what this is about if you actually read it. They are setting up a registry to help evaluate the effectiveness and safety of class II implantable and class III medical devices. What is a class III medical device? A class III device is one for which insufficient information exists to assure safety and effectiveness solely through the general or special controls sufficient for Class I or Class II devices. Such devices will include replacement heart valves, silicone gel-filled breast implants, implanted cerebral stimulators, and implantable pacemaker pulse generators. That's all this is, nothing more. You can set your foil caps aside now, all is well for the moment.

    • donotfear profile image

      donotfear 8 years ago from The Boondocks

      Uh-oh! Lets bring on the de-magnitizers!

    • borge_009 profile image

      borge_009 8 years ago from Philippines

      Just like we see in movies.

    • Froggy213 profile image

      Greg Boudonck 8 years ago from Returned to an Isla Del Sol - Puerto Rico Will Rise Strong

      I hear you no one, but these chips are so small, finding it may be a problem--I wonder if magnets may render it useless though.

    • profile image

      no one 8 years ago

      I voted no in the poll, because if I ever find out that I have been implanted with one, it will be taken ands, ifs or buts!

    • tony0724 profile image

      tony0724 8 years ago from san diego calif

      Froggy I realize that we are having our rights removed from us in rapid fashion. And this has been going on in the smallest of increments over the last few decades. Now the powers that be are not even trying to hide it anymore and are blatantly and brazenly thumbing their noses at us. This is just to damn scary to contemplate. And in order to chip me I have no problem saying one of em will have a busted nose in the process.

    • Enlydia Listener profile image

      Enlydia Listener 8 years ago from trailer in the country

      I am not sure but I think they could do it with an ordinary IM when supposedly giving you a tetanus shot...we need to have the aid of some good scientists on our side who can tell you how to de-activate the chips

    • Froggy213 profile image

      Greg Boudonck 8 years ago from Returned to an Isla Del Sol - Puerto Rico Will Rise Strong

      I wish it was just a movie. Thanks breakfastpop.

    • breakfastpop profile image

      breakfastpop 8 years ago

      Oh how horrible. This is something out of a very bad grade B movie. This is so sick. Thanks for the info.

    • profile image

      DaVonna 8 years ago

      My husband says they have wanted to do this to the military for awhile. They will have to have some good running shoes on to put one in me. I know try it on the illegals first and see what happens.


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