Introduction CDSCO Registration for BP Monitor is mandatory under India’s Medical Device Rules, 2017, before any blood pressure monitor — manual, digital, or ambulatory — can be manufactured, imported, sold, or distributed in the country. CDSCO classifies the BP monitor as a Class B (low-to-moderate risk) medical device, so it [...]
Introduction CDSCO X-Ray Machine Registration in India is mandatory under the Medical Devices Rules (MDR) 2017. X-ray machines are classified as Class A, B, C, or D medical devices depending on risk level. Importers must obtain MD-14 (application) and MD-15 (import license). Manufacturers need MD-3/MD-5 for Class A/B or MD-7/MD-9 [...]
Introduction CDSCO Korean face serum registration in India follows two paths. For importing Korean-made serums, you submit a COS-1 application and receive COS-2 Grant of Import License. For manufacturing Korean-formulated serums in India, you apply via COS-5 and receive COS-8 Grant of Manufacture License. Both processes require product safety data, [...]
Introduction CDSCO medical device registration for surgical instruments is the mandatory approval process under the Medical Devices Rules, 2017, that lets a business manufacture, import or sell surgical instruments in India. Instruments are classified as Class A (low risk), B (low-moderate), C (moderate-high) or D (high risk) based on intended [...]
What is BIS CRS Registration for Wireless Keyboards? BIS CRS Registration for Wireless Keyboards is mandatory certification under the Electronics and Information Technology Goods (Requirement of Compulsory Registration) Order, 2021 (CRO 2021). Every wireless keyboard — whether made in India or imported — must carry a valid BIS Registration Certificate [...]
Introduction Cosmetic Manufacturing License Registration is the mandatory State-level approval under the Cosmetics Rules, 2020 to legally manufacture cosmetics and makeup in India. Applicants file Form COS-5 (Form COS-6 for a loan license) with their State Licensing Authority on the SUGAM portal, along with a GMP self-declaration in Form COS-7. [...]
Introduction CDSCO medical device registration for wheelchairs in India is mandatory under the Medical Devices Rules, 2017. Wheelchairs are classified as Class A, B, C, or D based on risk. Importers apply via Form MD-14 and receive a grant through Form MD-15. Domestic manufacturers use MD-3 (Class A/B, licensed by [...]
Introduction CDSCO medical device registration hospital beds in India is mandatory under the Medical Devices Rules, 2017. Hospital beds are classified as Class A, B, C, or D depending on risk. Importers apply via Form MD-14 and receive a grant through MD-15. Domestic manufacturers use Form MD-3 (Class A/B, licensed [...]
Introduction Patient monitors are notified medical devices under the Medical Devices Rules, 2017. They fall under Class A, B, C, or D depending on risk level. Importers need CDSCO licenses via Form MD-14 (application) and MD-15 (license grant). Manufacturers require MD-3/MD-5 for Class A & B and MD-7/MD-9 for Class [...]
CDSCO K-Beauty product registration follows two separate pathways depending on whether the products are imported or manufactured in India. For imported Korean cosmetics, the Indian agent, subsidiary, or importer files Form COS-1 on the CDSCO SUGAM portal; once CDSCO reviews the formulation, labelling, and Free Sale Certificate, it issues the [...]
