The Ministry of Health and Family Welfare has, vide Notification dated 16th October 2019, after consultation with the Drugs Technical Advisory Board, specified that the Ultrasound equipment device intended for external or internal use in human beings qualifies as “Drug” under section 3(b) of the Drugs and Cosmetics Act, 1940 (Sec 3b-Defines Drugs) with effect from November 01, 2019.
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