Other

Parts and accessories for ionising radiation apparatus

CDSCO CLEARANCE · CPCB CLEARANCE · +1 OTHER PGAS

HSN 9022 90 90 covers other parts and accessories for apparatus based on ionising radiations, and import 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 concurrently for covered product categories including PET and radiotherapy equipment.

What this is

HSN code

9022 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 notification)

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 that the medical device or accessory is registered with the Central Drugs Standard Control Organisation per the conditions in G.S.R. 102(E) dated 11-02-2020, issued by the Ministry of Health and Family Welfare. Upload the certificate of analysis (document code 0010dc), batch release certificate (document code 0030dc), and label of consignment (document code 0110dc) in e-Sanchit before the bill of entry is filed.
G.S.R. 102(E) dated 11-02-2020 (MOHFW) · CDSCO registration conditions
2
Obtain Extended Producer Responsibility authorisation from the Central Pollution Control Board for import of positron emission tomography (PET) equipment, radiotherapy equipment, and their accessories listed in Schedule I of the E-Waste (Management) Rules, 2022. EPR authorisation is not required for micro-enterprises as defined under the MSMED Act, 2006.
G.S.R. 801(E) dated 02-11-2022 · Schedule I, E-Waste (Management) Rules, 2022

A word of counsel

The most common error on this tariff line is treating EPR authorisation as optional on the assumption that the product is not end-of-life waste. CPCB's E-Waste (Management) Rules, 2022 apply at the import stage — EPR authorisation must be in place before the bill of entry, not after. Importers that are not micro-enterprises under the MSMED Act, 2006 and fail to upload CPCB-EPR credentials face detention of the consignment pending authorisation, with demurrage and ground rent accruing through the verification period.

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Frequently asked

Does HSN 9022 90 90 require BIS certification?

No, no BIS Quality Control Order covers this residual category of ionising-radiation apparatus parts and accessories. Import is governed by Central Drugs Standard Control Organisation registration under G.S.R. 102(E) dated 11-02-2020 and Central Pollution Control Board EPR authorisation under the E-Waste (Management) Rules, 2022.

Which document codes must be uploaded in e-Sanchit for this tariff line?

Three mandatory documents must be uploaded before out-of-charge: certificate of analysis — drug (0010dc), batch release certificate (0030dc), and label of consignment (0110dc).

Does the EPR authorisation requirement apply to all importers under this HSN?

No. EPR authorisation under G.S.R. 801(E) dated 02-11-2022 does not apply to micro-enterprises as defined in the MSMED Act, 2006; all other importers of the covered PET and radiotherapy equipment and accessories must hold a current CPCB-EPR authorisation at the time of import.

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