Parts and accessories

Parts and accessories for automatic regulating instruments

CDSCO CLEARANCE · MOHFW CLEARANCE

HSN 9032 90 00 (Parts and accessories for automatic regulating or controlling instruments) is subject to Central Drugs Standard Control Organisation (CDSCO) registration requirements under G.S.R. 102(E) dated 11-02-2020, issued by the Ministry of Health and Family Welfare (MOHFW). Import of medical devices listed in that notification is permitted only upon compliance with the registration and conditions specified therein.

What this is

HSN code

9032 90 00

Chapter

90 · Optical, photographic, measuring, checking, precision, medical or surgical instruments

Primary regulator

CDSCO · Medical Devices Rules (G.S.R. 102(E) dated 11-02-2020)

Customs documentation

Registration certificate from CDSCO
Import declaration from MOHFW
Compliance documentation from CDSCO

Applicable Partner Government Agencies

CDSCOCDSCO·Central Drugs Standard Control Organisation

MOHFWMOHFW·Ministry of Health and Family Welfare

Compliance steps

1
Confirm whether the specific parts and accessories being imported are listed medical devices under G.S.R. 102(E) dated 11-02-2020. If listed, obtain the requisite CDSCO registration before filing the bill of entry; consignments of listed devices without valid registration are liable to detention and confiscation.
G.S.R. 102(E) dated 11-02-2020, Ministry of Health and Family Welfare
2
Upload the CDSCO registration certificate and all compliance documentation mandated under G.S.R. 102(E) in e-Sanchit prior to out-of-charge. Ensure the registration covers the specific device category to which the parts and accessories belong.
G.S.R. 102(E) dated 11-02-2020, Ministry of Health and Family Welfare

A word of counsel

The most common error on this tariff line is assuming that 'parts and accessories' fall outside the CDSCO device-registration net because they are not finished instruments. G.S.R. 102(E) dated 11-02-2020 applies to parts and accessories of listed medical devices and the registration obligation attaches at the component level — an importer who clears unlisted sub-components of a regulated device without CDSCO registration faces the same detention and confiscation exposure as an importer of the finished device.

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Frequently asked

Does HSN 9032 90 00 require BIS certification?

No, no BIS Quality Control Order covers this tariff line. Import is governed by the Central Drugs Standard Control Organisation registration regime under G.S.R. 102(E) dated 11-02-2020 issued by the Ministry of Health and Family Welfare, applicable where the goods qualify as listed medical devices or their parts.

How does an importer determine whether specific parts and accessories fall within the G.S.R. 102(E) listed-device scope?

The importer must cross-reference the goods against the device categories enumerated in G.S.R. 102(E) dated 11-02-2020; where the parts or accessories are integral to a listed medical device, CDSCO registration is mandatory before import.

What happens if a consignment of parts and accessories arrives without CDSCO registration for a listed device category?

The consignment is liable to detention at the port of entry; absent rectification by submission of valid registration, the goods are subject to confiscation and the importer faces monetary penalty under the applicable provisions of the Medical Devices Rules.

Last verified against gazette notifications: 2026-05-16. Source: CDSCO / MOHFW / Indian Customs CUSDATA.