For other uses

Ionising radiation apparatus for non-medical industrial uses

CDSCO CLEARANCE · CPCB CLEARANCE · +1 OTHER PGAS

HSN 9022 29 00 (apparatus based on ionising radiations, for other uses) 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), as a listed medical device condition applied to this tariff line. The Central Pollution Control Board (CPCB) Extended Producer Responsibility (EPR) authorisation under Schedule I of the E-Waste (Management) Rules, 2022 applies concurrently for radiotherapy equipment and accessories, with a carve-out for MSME micro-enterprises.

What this is

HSN code

9022 29 00

Chapter

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

Primary regulator

CDSCO · G.S.R. 102(E) dated 11-02-2020 (MOHFW medical device registration conditions)

Customs documentation

Registration certificate from CDSCO
EPR authorisation from CPCB
Certificate of analysis from manufacturer

Applicable Partner Government Agencies

CDSCOCDSCO·Central Drugs Standard Control Organisation

CPCBCPCB·Central Pollution Control Board

MOHFWMOHFW·Ministry of Health and Family Welfare

Compliance steps

1
Confirm the device is registered with the Central Drugs Standard Control Organisation under the conditions specified in G.S.R. 102(E) dated 11-02-2020. Upload the mandatory documents — certificate of analysis (document code 0010dc), batch release certificate (document code 0030dc), and label of consignment (document code 0110dc) — in e-Sanchit before filing the bill of entry.
G.S.R. 102(E) dated 11-02-2020 issued by Ministry of Health and Family Welfare · document codes 0010dc, 0030dc, 0110dc
2
Obtain Extended Producer Responsibility authorisation from the Central Pollution Control Board before import of radiotherapy equipment and accessories covered under Schedule I of the E-Waste (Management) Rules, 2022. The EPR obligation does not apply to micro-enterprises as defined under the MSME Development Act, 2006.
G.S.R. 801(E) dated 02-11-2022 · Schedule I of the E-Waste (Management) Rules, 2022

A word of counsel

The most common error on this tariff line is treating the CDSCO registration condition as inapplicable on the basis that the goods are classified as 'for other uses' rather than medical. The G.S.R. 102(E) registration conditions applied by MOHFW attach at the tariff-line level; an importer who ships without CDSCO registration and the three mandatory e-Sanchit documents faces consignment detention and customs out-of-charge refusal even when the EPR authorisation from CPCB is current.

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Frequently asked

Does HSN 9022 29 00 require BIS certification?

No, no BIS Quality Control Order covers this apparatus sub-category. Import is governed by Central Drugs Standard Control Organisation registration conditions under G.S.R. 102(E) dated 11-02-2020, with an Extended Producer Responsibility overlay administered by the Central Pollution Control Board under the E-Waste (Management) Rules, 2022.

Which documents must be uploaded in e-Sanchit at the bill of entry stage?

Three documents are mandatory: certificate of analysis (document code 0010dc), batch release certificate (document code 0030dc), and label of consignment (document code 0110dc); customs out-of-charge will be withheld if any of these are missing from e-Sanchit.

Is the CPCB EPR authorisation required for all importers of radiotherapy equipment?

No. The EPR authorisation under G.S.R. 801(E) dated 02-11-2022 does not apply to micro-enterprises as defined in the MSME Development Act, 2006; all other importers of radiotherapy equipment and accessories listed in Schedule I of the E-Waste (Management) Rules, 2022 must obtain it before import.

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