Datrend Systems Inc. has been assessed and registered by Intertek as conforming to the requirements of ISO13485:2016. The quality management system is applicable to design, manufacture and servicing of electronic equipment for medical applications and for the testing of medical equipment.
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Datrend subscribes to the regulatory standards of CSA, UL, and the EU.
Products are designed and manufactured following the quality system principles of ISO and FDA QSR/cGMP.
Datrend’s Quality System is registered to ISO13485:2016.