Saturday, October 9, 2010

MRS 2000 Now Registered With The FDA




From time to time people ask if the MRS 2000 is registered with the FDA in the US. Originally, although it had been inspected and accepted by the FDA, MediConsult, the manufacturer of the MRS 2000, did not seek to be registered by the FDA. Now it has done that and is officially registered with the FDA. You can check this at the FDA's own website, http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=222697&1pcd=ISA.
It is also interesting to note that our 2 closest competitors, the Bemer 3000 and the QRS are not registered with the FDA. It should also be noted that the MRS 2000 is only one of 2 Pulsating Electromagnetic Field Therapy (PEMFT) devices registered with the FDA and the other one costs $25,000.
To find out more about the MRS 2000 and the other products from MediConsult please go to my website www.mrs2000.ca or you can email me at DSKLARC608@rogers.com or call me toll free from anywhere in the continental US or Canada at, 1-866-551-0055. Because of government restrictions, MediConsult reps are not allowed to publish the prices of the equipment. Please contact me for the prices of the equipment you are interested in.

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