Earlier this year, the Central Drugs Standard Organisation (CDSCO) had set the October 1 deadline for bringing class C and class D medical devices under regulation to control quality. According to the new regulation, medical devices belonging to these categories, such as ventilators, imagining equipment, oxygen therapy equipment, nebulisers, x-ray equipment, surgical robots and oncology treatment linear accelerator, can t be sold from October 1 without a manufacturing licence.
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