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 [...]
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, [...]
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 [...]
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 [...]
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 [...]
