Dynatec Bioburden Procedures, Include the Analysis of Medical Devices for:
Dynatec utilizes the latest United States Pharmacopeia Guidelines, as well as the current Association for the Advancement of Medical Instrumentation (AAMI), Standards in all their testing. Dynatec utilizes Bioburden data to qualify your Medial Device for VDmax, AAMI Method 1, and a host of commercial sterilization related processes. Dynatec complies with AAMI ISO 11137, ISO 11737, and a host of other related standards. “Bioburden Identification” Dynatec qualified staff, utilize a host of methods for the identification, and characterization of your products Bioburden microbial population. Methods Include:
Dynatec's staff is available to assist you with your Bioburden Testing needs. Call 915-849-1322 (ext. 111) or email us. |
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| Dynatec Scientific Laboratories, is the Medical Device Laboratory which holds "THE KEY TO MARKET ADVANTAGE". From product development to regulatory compliance...Let Dynatec do it all for you!  Dynatec is registered with the FDA #16453338 |
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News Dynatec is now ACLASS Accredited to ISO 17025: 2005 #AT-1372 Click here to view certificate  Dynatec third party lab for air compressor certification to ISO 8573 via TUV America.  
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