Other

Parts and accessories for electrical measuring instruments

CDSCO CLEARANCE · MOHFW CLEARANCE

HSN 9030 90 90 (parts and accessories for oscilloscopes, spectrum analysers and other electrical measuring 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), where the part or accessory falls within the notified medical-device categories. Importers must confirm whether the specific item is captured by the G.S.R. 102(E) schedule before filing the bill of entry.

What this is

HSN code

9030 90 90

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, MOHFW)

Customs documentation

Registration certificate from CDSCO
Import licence from CDSCO
MOHFW G.S.R. 102(E) compliance declaration

Applicable Partner Government Agencies

CDSCOCDSCO·Central Drugs Standard Control Organisation

MOHFWMOHFW·Ministry of Health and Family Welfare

Compliance steps

1
Verify whether the specific part or accessory falls within the medical-device categories notified under G.S.R. 102(E) dated 11-02-2020. Where it does, obtain the requisite CDSCO registration before the bill of entry is filed; import without valid registration is a violation of the conditions prescribed in that notification.
G.S.R. 102(E) dated 11-02-2020, Ministry of Health and Family Welfare
2
Upload the CDSCO registration certificate and any other mandatory documents prescribed under G.S.R. 102(E) in e-Sanchit at the bill of entry stage. Customs out-of-charge will not be granted for notified medical-device parts where the CDSCO registration evidence is absent or expired.
G.S.R. 102(E) dated 11-02-2020, Ministry of Health and Family Welfare · CDSCO registration conditions

A word of counsel

The single most common error on this tariff line is assuming that because the 8-digit description reads 'Other' under parts and accessories, the product sits outside the medical-device regulatory perimeter. G.S.R. 102(E) captures parts and accessories of notified devices, and a component that functions as part of a regulated measuring or detecting instrument may independently require CDSCO registration — detention at the port of import follows if that determination is made first by the customs proper officer rather than by the importer.

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Frequently asked

Does HSN 9030 90 90 require BIS certification?

No, no BIS Quality Control Order covers this parts-and-accessories residual tariff line. Import is instead governed by Central Drugs Standard Control Organisation registration requirements under G.S.R. 102(E) dated 11-02-2020, issued by the Ministry of Health and Family Welfare, where the item falls within the notified medical-device schedule.

How do I determine whether my specific part or accessory requires CDSCO registration under G.S.R. 102(E)?

The registration obligation applies to parts and accessories of medical devices listed in G.S.R. 102(E) dated 11-02-2020; the importer must check the notified device categories against the intended use and function of the imported item before filing the bill of entry.

What are the consequences of importing a notified medical-device part without CDSCO registration?

Import without the registration and compliance conditions mandated by G.S.R. 102(E) exposes the consignment to detention at the port of entry and the importer to regulatory enforcement action by CDSCO under the applicable provisions of the Medical Devices Rules.

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