ObamaCare includes mandatory microchip implant for everyone since March 2013 | |
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BS Smeller
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Phoenix 2012
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Anonymous Coward User ID: 33152890 United States 02/11/2013 02:52 PM Report Abusive Post Report Copyright Violation | I think I found it... "‘‘National Medical Device Registry 21 ‘‘(g)(1) The Secretary shall establish a national med- 22 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 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 Coordi- 9 nator for Health Information Technology, and the Sec- 10 retary of Veterans Affairs, determine the best methods 11 for— 12 ‘‘(A) including in the registry, in a manner con- 13 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 iden- 16 tifier;" ? Under subtitle C, page 1000-1001-1002 |
Anonymous Coward User ID: 33464643 United States 02/11/2013 02:53 PM Report Abusive Post Report Copyright Violation | I think I found it... Quoting: Anonymous Coward 33152890 "‘‘National Medical Device Registry 21 ‘‘(g)(1) The Secretary shall establish a national med- 22 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 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 Coordi- 9 nator for Health Information Technology, and the Sec- 10 retary of Veterans Affairs, determine the best methods 11 for— 12 ‘‘(A) including in the registry, in a manner con- 13 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 iden- 16 tifier;" ? Under subtitle C, page 1000-1001-1002 Yup, this is what people are calling the mark. I know I'm not taking it lol. |
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Brad Daylight
User ID: 1779676 United States 02/11/2013 09:27 PM Report Abusive Post Report Copyright Violation | It isn't there, I used CTRL + F and read through, nothing about microchips. "I have felt despair many times in my life, but I do not keep a chair for it." ~Dr. Clarissa Pinkola Estes Today is a gift, that is why it is called "The Present" “When an opponent declares, “I will not come over to your side,” I calmly say, “Your child belongs to us already… What are you? You will pass on. Your descendants, however, now stand in the new camp. In a short time they will know nothing else but this new community.” - Adolf Hitler “If you want to tell people the truth, make them laugh, otherwise they'll kill you.” -Oscar Wilde Have a nice day, may God bless you :D |
Anonymous Coward User ID: 28870983 United States 02/11/2013 09:28 PM Report Abusive Post Report Copyright Violation | I think I found it... Quoting: Anonymous Coward 33152890 "‘‘National Medical Device Registry 21 ‘‘(g)(1) The Secretary shall establish a national med- 22 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 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 Coordi- 9 nator for Health Information Technology, and the Sec- 10 retary of Veterans Affairs, determine the best methods 11 for— 12 ‘‘(A) including in the registry, in a manner con- 13 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 iden- 16 tifier;" ? Under subtitle C, page 1000-1001-1002 Yup, this is what people are calling the mark. I know I'm not taking it lol. all they have to do is require a swipe of your chip before you can renew your drivers license or license plate tags. they will easily enforce it.... |
Anonymous Coward User ID: 20063594 United States 02/11/2013 09:47 PM Report Abusive Post Report Copyright Violation | |
Anonymous Coward User ID: 20063594 United States 02/11/2013 09:55 PM Report Abusive Post Report Copyright Violation | i belive it has to do with geting the fda to give to OK stamp on devices that work vs BUNK devices that why you see those comercials do you or a loved one have this or that hip replacement or this or that knee replacement or a certian type of pacemakers ect ect ect if so contatack xxxxxxlawfirm ect if that the case with that ? and what excatly is a class 2 and 3 device ? pacemaker hip replacement ect ect ? again im not sure what all this is it just my opinion i could be flat out wrong and it could me LINE UP AND TAKE THE MARK so am i right or wrong? the reason why i think it refers to devices like pacemakers and knee/hip replacement ect is because thats what i was told after i posted the same BILL on a different fourm, and asked if people think this means the MARK or not. and a few people said itsthose types of devices. so what say you ? |
Anonymous Coward User ID: 20063594 United States 02/11/2013 10:01 PM Report Abusive Post Report Copyright Violation | holy shit i googled what a madical device is trying to debunk my above staments and yup Medical devices incorporating RFID In 2004, the FDA authorized marketing two different types of medical devices that incorporate radio-frequency identification, or RFID. The first type is the SurgiChip tag, an external surgical marker that is intended to minimize the likelihood of wrong-site, wrong-procedure and wrong-patient surgeries. The tag consists of a label with passive transponder, along with a printer, an encoder and a RFID reader. The tag is labeled and encoded with the patient's name and the details of the planned surgery, and then placed in the patient's chart. On the day of surgery, the adhesive-backed tag is placed on the patient's body near the surgical site. In the operating room the tag is scanned and the information is verified with the patient's chart. Just before surgery, the tag is removed and placed back in the chart. The second type of RFID medical device is the implantable radiofrequency transponder system for patient identification and health information. One example of this type of medical device is the VeriChip, which includes a passive implanted transponder, inserter and scanner. The chip stores a unique electronic identification code that can be used to access patient identification and corresponding health information in a database. The chip itself does not store health information or a patient's name so at this point im gonna have to say ITS THE MARK OF THE BEAST fuck fuck fuck |
Anonymous Coward User ID: 29130092 United States 02/11/2013 10:02 PM Report Abusive Post Report Copyright Violation | I think I found it... Quoting: Anonymous Coward 33152890 "‘‘National Medical Device Registry 21 ‘‘(g)(1) The Secretary shall establish a national med- 22 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 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 Coordi- 9 nator for Health Information Technology, and the Sec- 10 retary of Veterans Affairs, determine the best methods 11 for— 12 ‘‘(A) including in the registry, in a manner con- 13 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 iden- 16 tifier;" ? Under subtitle C, page 1000-1001-1002 Ding Ding Ding And I'm not taking it.. Will starve to death if I have to. |
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Anonymous Coward User ID: 34208580 United States 02/11/2013 10:32 PM Report Abusive Post Report Copyright Violation | There are three classes of medical devices, I through III, and the higher the class the more regulations the device has. Class I medical devices are the basics. Things that fall into this category include bandages, examination gloves and tongue depressors. Nearly half of all medical devices are Class I, and almost all of them are exempt from regulations [source: FDA]. Class II medical devices make up most of the other half, and include products such as amalgam dental fillings, infusion pumps, apnea monitors, and cardiac monitors. They are a little bit riskier than Class I-designated products and sometimes have special requirements such as with their labeling or performance standards. When we get to the Class III devices, we're usually talking about cutting-edge medical breakthroughs, new technologies and devices that are too new to know how safe they may be. These might include life-support and life-sustaining systems, some of which are implantable. Drug-eluting coronary stents (which slowly release medication after implantation) and intra-aortic balloon pumps, for example, are Class III devices, but so are breast implants because they carry a health and safety risk. Some Class III devices such as drug-eluting stents, for example, already have their own tracking registry. About 10 percent of medical devices are considered Class III [source: FDA]. The idea behind the registry was to track the safety and effectiveness of these medical devices after they're already on the market -- there's where the word surveillance comes in -- especially those that are implanted inside of a person, such as hip replacements (and other orthopedic implants) and pacemakers. This is key: The registry would not have been linked to your identifiable personal information or medical records, but it would have provided data for statistical analysis to link, for example, a mechanical issue in hip replacement systems with faster and more effective patient notification and treatment. |
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