CDSCO Registration for Defibrillator: Class C License, Forms & Process (2026 Guide) For Importers, Manufacturers & Wholesalers

Introduction CDSCO Registration for Defibrillator is mandatory under India’s Medical Device Rules, 2017, before any defibrillator — automated external (AED), manual external, or related cardiac-shock device — can be manufactured, imported, sold, or distributed in the country. CDSCO classifies the defibrillator as a Class C (moderate-to-high risk) medical device because [...]

CDSCO Medical Device License for Dialysis Machine: Complete 2026 Guide For Manufacturer, Importer & Wholesaler

Introduction A CDSCO medical device license for dialysis machine is mandatory before manufacturing, importing, or selling any haemodialysis or peritoneal dialysis machine in India. CDSCO classifies the standalone Dialysis Machine as a Class C medical device under the Medical Device Rules, 2017 — used for acute or chronic kidney failure [...]

EPR Registration Process on the CPCB Portal: Step-by-Step Guide (Plastic, E-Waste, Battery, Tyre & Used Oil)

Introduction The EPR Registration Process on the CPCB Portal involves creating an account on the relevant category-specific portal (Plastic, E-Waste, Battery, Tyre, or Used Oil), submitting Form I with company and product details, declaring an EPR Action Plan for collection and recycling, uploading supporting documents, paying the registration fee online, [...]

LMPC Registration for Manufacturers: Complete 2026 Guide

Introduction LMPC registration for manufacturers is the mandatory approval under Rule 27 of the Legal Metrology (Packaged Commodities) Rules, 2011 for any business that produces and pre-packs a commodity for sale in India. Under Rule 2(d), “manufacturer” includes not just the entity that physically makes the product, but also a [...]

LMPC Registration in India: The Complete Guide (2026)

Introduction LMPC registration is the mandatory approval under Rule 27 of the Legal Metrology (Packaged Commodities) Rules, 2011 that every manufacturer, packer, and importer of pre-packaged goods must obtain before selling in India. It registers your business name and address with the state Controller (or Director) of Legal Metrology and [...]

CDSCO License for Oxygen Concentrator: Complete Guide to Registration, Forms & Compliance in India (2026)

Introduction An oxygen concentrator is a Class B medical device under MDR 2017, requiring CDSCO registration before manufacture, import, or sale in India. Manufacturers need Form MD-3 (application) and MD-5 (license) for Class A/B devices. Importers apply via MD-14 and receive MD-15. Wholesale distributors use MD-41 and receive MD-42. All [...]

BIS Certification for Rigid PVC Sheets: Complete IS 6307:2023 Compliance Guide

Introduction BIS certification for rigid PVC sheets is the ISI mark approval issued by the Bureau of Indian Standards to manufacturers of rigid PVC sheets under the updated Indian Standard IS 6307:2023. Manufacturers apply on the BIS Manak Online portal, submit factory and product documents, undergo a factory inspection and [...]

FSSAI License Modification: Complete 2026 Guide to Updating Your License Details

Introduction FSSAI license modification is the process of updating the details on your existing, still-valid FSSAI license or registration — such as your business address, Kind of Business, product categories, directors/partners, or ownership — through the FoSCoS portal. It’s different from renewal, which is about extending a license before it [...]

Cosmetic Import Registration in India: The Complete Journey for Foreign Brands (COS-1 to COS-2 Guide, 2026)

Introduction Cosmetic import registration in India is the mandatory approval a foreign brand needs before its cosmetics can be imported, cleared through customs, and sold in India, under Rule 12(1) of the Cosmetics Rules, 2020. Since a foreign manufacturer cannot apply directly, the journey starts with appointing an authorized Indian [...]

CDSCO MD-14 Endorsement Registration: Complete Guide to Adding Devices to Your Import License

Introduction CDSCO MD-14 endorsement registration is the process importers use to add new medical devices, models, or manufacturing sites to an already-granted Form MD-15 import license, without applying for a brand-new license from scratch. You file a fresh Form MD-14 application along with the existing import license copy, an updated [...]

Author: jyotisharma