RFID BY ANY OTHER NAME-2017
This has been in the works for many years. It’s not a figment of people’s imagination, nor is it conspiracy. IT’S REAL. IT’S HERE. IT’S NOW. It’s said the REAL implementation will begin in 2017. The tracking of us all!
National Medical Device Industry
Health Care Bill
Don’t think they’ve left our children out, either! Page 993-School Based Health Clinics
In Vitro Diagnostic (IVD) Device Studies
In vitro diagnostics (IVDs) meet the definition of a device under the Act. Section 201(h) of the Act defines a device as:
“an instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar or related article, including any component, part, or accessory, which is—
(1) recognized in the official National Formulary, or the United States Pharmacopeia, or any supplement to them,
(2) intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation, treatment, or prevention of disease, in man or other animals, or
(3) intended to affect the structure or any function of the body of man or other animals, and which does not achieve its primary intended purposes through chemical action within or on the body of man or other animals and which is not dependent upon being metabolized for the achievement of its primary intended purposes.” 21 U.S.C. 321(h) (emphasis added).
(d)Implant means a device that is placed into a surgically or naturally formed cavity of the human body if it is intended to remain there for a period of 30 days or more. FDA may, in order to protect public health, determine that devices placed in subjects for shorter periods are also “implants” for purposes of this part.
UDI-Unique Device Indentification
Medical Device Registry
Do you think these devices are place within your body and not monitored? Think again!
Medical Device Registries Task Force & Postmarket Surveillance System