Microtomes, including parts and accessories thereof
Microtomes and their parts and accessories
HSN 9027 90 10 (Microtomes, including parts and accessories thereof) 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). Central Pollution Control Board (CPCB) Extended Producer Responsibility authorisation under the E-Waste (Management) Rules, 2022 applies as a concurrent overlay for importers of electronic analysers and accessories.
- Registration certificate from CDSCO
- EPR authorisation from CPCB
- Import licence from MOHFW
- 1Verify that the microtome or accessory is listed in G.S.R. 102(E) dated 11-02-2020 and obtain the required CDSCO registration before filing the bill of entry. All conditions of registration specified in the MOHFW notification must be satisfied; non-compliant consignments are liable to detention at the port of import.G.S.R. 102(E) dated 11-02-2020 · Ministry of Health and Family Welfare notification
- 2Obtain Extended Producer Responsibility (EPR) authorisation from the Central Pollution Control Board for import of analysers and accessories falling under Schedule I of the E-Waste (Management) Rules, 2022, unless the importing entity qualifies as a micro enterprise under the MSMED Act, 2006. Upload evidence of EPR authorisation or micro-enterprise exemption at the bill of entry.E-Waste (Management) Rules, 2022 · G.S.R. 801(E) dated 02-11-2022
- 3For used or refurbished high-end, high-value medical equipment (other than critical care medical equipment), comply with the conditions specified in the Office Memorandum issued by the Ministry of Environment, Forest and Climate Change dated 15-12-2023. Import of such equipment is restricted and subject to additional approvals.O.M. issued by Ministry of Environment, Forest and Climate Change dated 15-12-2023
The most common error on this tariff line is overlooking the EPR authorisation obligation on the assumption that it applies only to consumer electronics. Schedule I of the E-Waste (Management) Rules, 2022 covers laboratory analysers and their accessories, and the CPCB authorisation must be in place before import — not retrospectively applied after clearance. Micro-enterprise status under the MSMED Act, 2006 is the only recognised exemption from EPR, and the burden of demonstrating that status rests on the importer at the bill-of-entry stage.