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I forwarded these links to friends and family...You should create a new thread with this one
Originally posted by angelx666
Microchip implants ready for use with swine flu vaccine
Verichip partnered with Minnesota (Minnesota again?) to develop swine chip
REUTERS www.reuters.com...
Next step in H1N1 scare: Microchip implants
WND www.wnd.com...
Full programme:
www.receptorsllc.com...
(personal opinion: if they even mentioned this in the bill- its coming)
Originally posted by conspiracyrus
reply to post by maybereal11
HAHA read the post and your sources bud, were talking about IMPLANTABLES ... CLASS 2 IMPLANTABLES ... not wheelchairs and such, and Class 2 implantables are almost EXCLUSIVELY, LIKE I SAID BEFORE, rfid type devices ...
Howmedica Osteonics Corporation
c/o Mr. Francisco Haro
Regulatory Affairs Specialist
325 Corporate Drive MAR 0 8 2007
Mahwah, New Jersey 07430
Re: K063552
Trade/Device Name: Series II Constrained Acetabular Liners
Regulation Number: 21 CFR 888.3310
Regulation Name: Hip joint metal/polymer constrained cemented or uncemented prosthesis
Regulatory Class: Class II
Product Code: KWZ
Dated: February 16, 2007
Received: February 20, 2007
Originally posted by Bombeni
reply to post by maybereal11
Did you buy a lot of stock in Verichip or something?
Originally posted by conspiracyrus
Class II implantables are almost exclusively RFID chips...
[edit on 1-9-2009 by conspiracyrus]
Originally posted by Bombeni
reply to post by maybereal11
Did you buy a lot of stock in Verichip or something?
Originally posted by conspiracyrus
reply to post by maybereal11
wow man really ... can you not read ...
JUST IN CASE YOU MISSED MY SOURCE ON THAT LAST INFORMATION I WILL CAPS THIS AND OFFER THE LINK AGAIN www.emergogroup.com...
[edit on 3-9-2009 by conspiracyrus]
Originally posted by conspiracyrus
reply to post by maybereal11
wow man really ... can you not read ... ... really guy you need to read the posts ... if you disagree with what im saying then find a source and read it to make sure it is up to date and actually supports what you say [edit on 3-9-2009 by conspiracyrus]
Originally posted by conspiracyrus
reply to post by maybereal11
You do realize that Mergo consults for people trying to get devices past the fda? and especially on the classification of medical devices?
[edit on 3-9-2009 by conspiracyrus]
the European Commission's Medical Device Expert Group, MDEG, endorsed a guidance document on this Directive at its December 2006 meeting. The guidance document was issued in January 2007 and is titled Guidance Document on Directive 2005/50/EC on the Reclassification of Hip, Knee, and Shoulder Joint Replacements. The Guidance document delineates the common interpretation by the Member States of Directive 2005/50/EC.