For projectors

Parts and accessories for cinematographic projectors

CDSCO CLEARANCE · MOHFW CLEARANCE

HSN 9007 92 00 (parts and accessories for cinematographic projectors) 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 article falls within the medical-device categories notified therein. Importers must confirm whether the specific part meets the notified medical-device definition before filing the bill of entry.

What this is

HSN code

9007 92 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 (MOHFW notification)

Customs documentation

Registration certificate from CDSCO
MOHFW notification compliance declaration
Import permit from CDSCO

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 listed in G.S.R. 102(E) dated 11-02-2020. If it does, obtain the requisite CDSCO registration before filing the bill of entry; unregistered import of a notified medical device attracts detention and monetary penalty.
G.S.R. 102(E) dated 11-02-2020 issued by the Ministry of Health and Family Welfare
2
Upload the CDSCO registration certificate and any other conditions of registration mandated by G.S.R. 102(E) in e-Sanchit at the bill-of-entry stage. Failure to upload mandatory PGA documents before out-of-charge will result in consignment detention pending verification.
G.S.R. 102(E) dated 11-02-2020; Medical Devices Rules (CDSCO registration conditions)

A word of counsel

The most common error on this tariff line is assuming that a cinematographic-projector part is categorically outside CDSCO scope because the heading is classified under optical/photographic instruments rather than medical devices. G.S.R. 102(E) can capture accessories and parts used with notified medical-imaging or projection devices regardless of the optical-instruments chapter placement; a scope assessment against the notified categories must be completed before placing the import order, not at the port gate.

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Frequently asked

Does HSN 9007 92 00 require BIS certification?

No, no BIS Quality Control Order covers parts and accessories for cinematographic projectors. Where the article meets the medical-device definition, import is governed by the Central Drugs Standard Control Organisation under G.S.R. 102(E) dated 11-02-2020 issued by the Ministry of Health and Family Welfare.

How do I determine whether my specific projector part falls under the G.S.R. 102(E) notified medical-device list?

Cross-check the part's intended use and description against the categories enumerated in G.S.R. 102(E) dated 11-02-2020; parts intended for general cinematographic use and not meeting the medical-device definition are outside CDSCO scope.

What happens if a projector accessory classified here is imported without CDSCO registration when registration is required?

Importation of a notified medical device without CDSCO registration renders the consignment liable to detention, seizure, and monetary penalty under the applicable Medical Devices Rules conditions specified in G.S.R. 102(E).

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