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In continuation to the draft classification list published previously in June 2017, CDSCO has now released an updated list taking into consideration industry inputs. This is another milestone towards the transition to the New Medical Device Rules, 2017 effective 1st January 2018.
Just to recap, CDSCO has classified the medical devices and in vitro diagnostic medical devices, based on the intended use of the device, risk associated with the device and other parameters specified in the First Schedule which is in line with the International classification. This is an extremely positive move by CDSCO providing clarity on the medical devices falling under the specific notified categories. This list can be used as a ready reckoner to easily identify the medical devices regulated in India.
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