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Solos Endoscopy and TUV SUD America Schedule Stage 1 ISO 13485 Audit for February 26, 2013
Date:1/24/2013

BOSTON, Jan. 24, 2013 /PRNewswire/ -- Solos Endoscopy, Inc. (OTCPK: SNDY) is pleased to announce that the Company and TUV SUD America has scheduled its Stage 1 ISO 13485 Audit for February 26, 2013.

Solos Endoscopy retained TUV SUD America, Inc. to complete its ISO 13485 Certification and Audit. The Company previously engaged Expert Resource to prepare the Company for the final audit, which will be conducted by TUV SUD America. 

TUV SUD Product Service is accredited by the ZLG in Bonn, Germany, as a Certification Body for quality management systems to the ISO 13485 standard. TUV SUD also holds accreditation with the Standards Council of Canada (SCC) and Health Canada for the Canadian Medical Devices Regulations. In addition, TUV SUD is a Notified Body for certification to all relevant EU Directives. With this complete service package, TUV SUD can assist medical companies in accessing markets nationally, in Europe, and globally. Solos Endoscopy has posted on its website an updated schedule as of January 2013. 

According to Solos Endoscopy, CEO, Robert Segersten , "Our team has been working diligently with Expert Resources and we believe that Solos will be prepared for the upcoming Audit in February."

Expert Resource will attend the final audit, and help interpret any findings.  Solos Endoscopy joins a high profile Expert Resource client list which includes BASF, Black & Decker, Dow Precision, Hitachi, J.D. Power & Associates, Microsoft Corporation, Northrop Grumman, Quest, and Toshiba, amongst many others. According to Expert Resource, their consultants maintain a 100% success rate of passing the final audit on the first attempt. Solos Endoscopy has posted its updated ISO 13485 CE Mark Schedule on its website, http://www.
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SOURCE Solos Endoscopy, Inc.
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