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What do they mean for Medical Design OEMs?
The standards for biocompatibility used by U.S. Pharmacopoeia (USP) Class VI standard and ISO 10993 standards can significantly impact your medical instrumentation development.
With the right knowledge, and by incorporating biocompatibility into your design, you can:
Reduce time for system integration
Avoid delays in product development
Improve the performance and efficiency of your instrument
Save time qualifying your application for compliance
In order to be considered biocompatible, no unwanted biological effects or after effects can result from using your medical instrument -- this includes all sub-components in your system. Is your application designed with this in mind?
Make sure you understand the standards.
Download the "Biocompatibility of Anesthesia / Respiratory Products" whitepaper and avoid delays in your product launch.
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