Optical fibres, optical fibres bundles and cables
Optical fibres, optical fibre bundles and cables
HSN 9001 10 00 (Optical fibres, optical fibre bundles and cables) is subject to Central Drugs Standard Control Organisation (CDSCO) registration under the Medical Devices Rules, 2017, where the product is listed in G.S.R. 102(E) dated 11-02-2020 issued by the Ministry of Health and Family Welfare (MOHFW). Telecom Equipment Certification under the Indian Telegraph (Amendment) Rules, 2017 and Department of Telecommunications Mandatory Testing and Certification of Telecom Equipment (MTCTE) notifications applies as an additional overlay where the product falls within the notified telecom product list.
- Registration certificate from CDSCO
- MTCTE certification from DoT
- Import compliance declaration from MOHFW
- 1Verify whether the specific optical fibre or cable product falls within the medical devices listed in G.S.R. 102(E) dated 11-02-2020 issued by MOHFW. If listed, obtain CDSCO registration covering the product prior to filing the bill of entry; import without valid registration attracts detention and confiscation under the Medical Devices Rules, 2017.G.S.R. 102(E) dated 11-02-2020 · Ministry of Health and Family Welfare · Medical Devices Rules, 2017
- 2Confirm whether the product is notified under the MTCTE mandatory certification regime. If so, ensure compliance with the Indian Telegraph (Amendment) Rules, 2017 and the DoT TEC notifications — TEC/01/2017-TC dated 04-07-2019 and 23-06-2020, as amended vide F.No.5-2/2021-TC/TEC/131 dated 13-06-2022 and F.No.5-2/2024-TC/TEC(Pt.1) dated 25-02-2025 — and obtain the mandatory MTCTE certificate before clearance.Indian Telegraph (Amendment) Rules, 2017 · DoT TEC/01/2017-TC dated 04-07-2019 and 23-06-2020 · F.No.5-2/2021-TC/TEC/131 dated 13-06-2022 · F.No.5-2/2024-TC/TEC(Pt.1) dated 25-02-2025
The most common error on this tariff line is failing to conduct a dual-regime scope check at the product-description level before filing. Optical fibres used in medical imaging or surgical applications may fall within the G.S.R. 102(E) medical-device list and trigger CDSCO registration, while the same physical product configured for telecommunications infrastructure triggers MTCTE certification — and a product straddling both applications may require both clearances simultaneously. Importing under only one clearance while the product is captured by the second regime results in consignment detention at the port of entry.