As per the chamber, importer/refurbisher and end users could earlier import refurbished or pre-owned high-end, high-value medical equipment with a no objection certificate from the ministry of environment, forests & climate change but from August 15 they require drug regulator Central Drugs Standard Control Organization (CDSCO) registration.
CDSCO clarified that in the absence of provision to issue registration for refurbished medical equipment under the Medical Device Rules (MDR) 2017, they have stopped processing the applications previously submitted by importer/refurbisher, according to the Ficci representation, seen by ET. – Kirtika Suneja
