
The MDR(EU
2017/745) is latest set of regulations that govern the production and
distribution of medical devices in Europe, which replaces the former
Medical Device Directive 93/42/EEC (MDD). The new regulations emphasize on the
following objectives:
-Greater
protection of public health
-Better
control and accessibility of technical documentation
-Greater
transparency and traceability of medical devices
-More
comprehensive labeling through the introduction of a UDI code and reporting of
device data to the European database EUDAMED
This
success on MDR certification demonstrate our exceptional quality standard,
outstanding product safety and effectiveness. Famidoc sticks to our vision for
providing accessible, reliable, and affordable health care products to the
families around the world.
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