Many high-risk medical device manufacturers stop production

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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