Microchip incert, after the new health reform
Skrevet: Søn Jun 14, 2020 8:38 amUS will engage the chip on humans soon.
http://www.theflucase.com/index.php?opt ... 64&lang=en
The new Health Care Bill, H.R. 3200, just passed by Congress has within it the requirement that all people thereunder shall be microchiped. The plans for this microchipping has been in the hooper going back to December of 2004.
Witness the actual FDA (Food and Drug Administration) document dated December 10, 2004 entitled Class II Special Guidance Document: Implantable Radiofrequency Transponder System for Patient Identification and Health Information. This ten page document may be read on the FDA website at
http://www.fda.gov/downloads/MedicalDev ... 072191.pdf
Now witness the wording within H.R. 3200, America's Affordable Health Choices Act of 2009 found on Congresses™ House Ways and Means website, http://waysandmeans.house.gov/media/pdf ... 001xml.pdf
On page 1001 is Subtitle C National Medical Device Registry which states, 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 … is or has been used in or on a patient…
http://www.theflucase.com/index.php?opt ... 64&lang=en
The new Health Care Bill, H.R. 3200, just passed by Congress has within it the requirement that all people thereunder shall be microchiped. The plans for this microchipping has been in the hooper going back to December of 2004.
Witness the actual FDA (Food and Drug Administration) document dated December 10, 2004 entitled Class II Special Guidance Document: Implantable Radiofrequency Transponder System for Patient Identification and Health Information. This ten page document may be read on the FDA website at
http://www.fda.gov/downloads/MedicalDev ... 072191.pdf
Now witness the wording within H.R. 3200, America's Affordable Health Choices Act of 2009 found on Congresses™ House Ways and Means website, http://waysandmeans.house.gov/media/pdf ... 001xml.pdf
On page 1001 is Subtitle C National Medical Device Registry which states, 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 … is or has been used in or on a patient…