MP Biomedicals Diagnostic Division has been committed to providing superior quality and service at competitive prices for more than 40 years. All our products are developed and produced under the strictest standards in our our ISO 9002 facilities in Orangeburg, New York and in Burlingame, California. The MP Biomedicals Diagnostics Division is now certified to ISO 13485:1996 under CMDCAS (Certificate No. 74 500 2265) and is in compliance with cGMP regulations, the European Medical Device Directive (IVDD 98/79/EC), and Canadian Medical Device Regulations (CMDR, 1998). Products manufactured by the Diagnostics Division are CE marked for sale into Europe.
We believe you will find our level of service to be superior to other suppliers in the industry and our pricing to be extremely competitive.
SLT Price at posting:
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