Viscometers
Viscometers for physical or chemical analysis
HSN 9027 89 10 (Viscometers) is subject to Central Drugs Standard Control Organisation (CDSCO) registration under G.S.R. 102(E) dated 11-02-2020 issued by the Ministry of Health and Family Welfare (MOHFW), where the device is listed as a notified medical device. Extended Producer Responsibility (EPR) authorisation under the E-Waste (Management) Rules, 2022 (G.S.R. 801(E) dated 02-11-2022) administered by the Central Pollution Control Board (CPCB) applies as an additional overlay, with import of used or refurbished high-value medical equipment subject to conditions notified by the Ministry of Environment, Forest and Climate Change (MEFCC).
- Registration certificate from CDSCO
- EPR authorisation from CPCB
- Import permission from MOHFW
- 1Verify whether the viscometer model is listed in G.S.R. 102(E) dated 11-02-2020 issued by the Ministry of Health and Family Welfare. If listed, obtain CDSCO registration covering the specific device before filing the bill of entry; import without registration constitutes a violation of the conditions prescribed in that notification.G.S.R. 102(E) dated 11-02-2020 · Ministry of Health and Family Welfare notification
- 2Obtain Extended Producer Responsibility authorisation from the Central Pollution Control Board for import of analysers and accessories covered under Schedule I of the E-Waste (Management) Rules, 2022, before the consignment arrives at port. EPR authorisation is not required for micro-enterprises as defined under the MSME Development Act, 2006.E-Waste (Management) Rules, 2022 · G.S.R. 801(E) dated 02-11-2022
- 3If importing used or refurbished high-value, high-end medical equipment, comply with all conditions prescribed in the Office Memorandum issued by the Ministry of Environment, Forest and Climate Change dated 15-12-2023. Critical care medical equipment is excluded from this restricted-import regime; confirm the device category before shipment.O.M. issued by Ministry of Environment, Forest and Climate Change dated 15-12-2023
The most frequent error on this tariff line is assuming that a viscometer used in an industrial or laboratory context is automatically outside the CDSCO medical-device regime. G.S.R. 102(E) dated 11-02-2020 defines the listed devices by function, not end-use declaration; if the instrument falls within the notified categories, CDSCO registration is mandatory regardless of the importer's intended application. An unregistered consignment is liable to detention and confiscation at the port of import pending regularisation.