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Letter: Facts about Obamacare’s Class II Implantable Device

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Posted: Thursday, September 6, 2012 12:00 am

I'm concerned that some Americans are calling parts of Obamacare (HR 4872) a myth, or rumor. So, I decided to research the truth for Class II Implantable (RFID tag) device. There will be a "Unique Device Identification System" which includes Class II Implantable devices; verifiable references below:

[1] CLASS II IMPLANTABLE DEVICE: Page 2057 of the bill lines 3, a Class II Implantable device

[2] FEDERAL FOOD, DRUG AND COMETIC ACT (21 U.S.C. 360i(f)): Page 2063 lines 1-3, a reference to the "Federal Food, Drug and Cosmetic Act" (aka the "Unique Device Identification System")

For reference to the Cosmetic Act see

For reference to the "Unique Device Identification System" (aka the Cosmetic Act) see Title 21 Food and Drugs,

[3] UNIQUE DEVICE IDENTIFICATION SYSTEM: Computer page 4/6 of Title 21 Food and Drugs for the "Unique Device Identification System" (aka the "Federal Food, Drug and Cosmetic Act (21 U.S.C. 360i(f))"), see

[4] PROPOSED RULE: Pages 34 and 36 of the bill describes the Federal Register website. Page 2057 says the Secretary consulted with the Commissioner of Food and Drugs developing the Registry. Because the Commissioner of Food and Drugs is the head of the Food and Drugs Administration is the reason the "Proposed Rule" (aka "Unique Device Identification System") was posted by the FDA on July 10, 2012. For pages 34 and 36 see For the Proposed Rule see


RFID: See Table of Contents section II.B.1 for Definitions, in the Proposed Rule, page 17/67

RFID tag: See Table of Contents section IX.B for UDI Labeling Requirements, page 40/67; and section IX.B for Form of a Unique Device Identifier on page 43/67

Let's stop this administration by voting them out. We're losing our privacy and freedom.

Jim White


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