Electro Interstitial Scanner

The Electo Interstitial Scan (EIS), also called ESG (Electro-Somatography), is a relatively small computerized, electro-medical system claimed to be safe, noninvasive, with no side-effects or adverse reactions, that performs scannings on human subjects taking 4 minutes and providing 3-D image models as well as hard copy text reports.

EIS scans are claimed to be reliable, scientifically-based, accurate, reproducible, and can be repeated several times at any frequency, allowing the practitioner to verify and control their therapy, follow-ups, prescription drug dosages, etc..

The device and system have been criticized for a lack of legal and scientific standing, as well as a lack of FDA approval.

Function

The EIS device purports to be a biosensor that analyzes 22 computer-segregated volumes of human interstitial fluid in vivo, by application of a negligible 1.28 V current between organs and tissue showing their function or dysfunction, objectively studying individual diseases, as well as pharmaceutical agent efficacy and all treatment protocols -- without practitioner interference or bias.

Certificates

* FDA : American FDA certificate: EIS-BF 481-8-2007 Valid until 17.08.2009
* CE : European Class LNE/G-MED CE 0459Device category:Computerized assisted system of screening and functional diagnosisNo. 1172/B5/1
* ISO : ISO 9001 : 2000 - NF EN ISO 13485 : 2004. No. 1172 / 9001–13485 / 1

Criticisms

The device manufacturers have been criticized for making misleading health and diagnostic claims. The device lacks legal and scientific standing, and lacks FDA approval: "It has not been cleared for marketing and is not legal to market in interstate commerce in the United States." [http://www.devicewatch.org/reports/eis/eis.shtml Electro Interstitial Scans, Another Test to Avoid] - Stephen Barrett]

A search of the PubMed database fails to show any scientific research on this device or system.

External links

* [http://www.ldteck.com/ LD Technology]