Identifying the means and methods by which the government will accomplish their task is less than speculative. Though the legislation itself does not mandate this technology to be used, as we reported five years ago, the implantation of Radio Frequency Identification chips (RFID) into all persons within the government’s healthcare system for purposes of “prevention, detection and treatment of diseases” is a primary objective of a number of government officials and industry proponents. Whether or not they will be successful in doing so remains to be seen.
Today, hospitals throughout America are already implementing RFID technology and have begun implanting RFID chips into their patients for medical purposes, such as those who suffer from Alzheimer.
The Obama Health care bill under Class II (Paragraph 1, Section B) specifically includes in it's lists of things that must be in registered in the NATIONAL MEDICAL DEVICE REGISTRY: ‘‘(ii) a class II device that is implantable."
Then on page 1004 it describes what the term "data" means in paragraph 1, section B:
14 ‘‘(B) In this paragraph, the term ‘data’ refers to in
15formation 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
What exactly is a class II device that is implantable? Lets see...
Approved by the FDA, a class II implantable device is a "implantable radiofrequency transponder system for patient identification and health information." The purpose of a class II device is to collect data in medical patients such as "claims data, patient survey data, standardized analytic files that allow for the pooling and analysis of data from disparate data environments, electronic health records, and any other data deemed appropriate by the Secretary."