<p dir="ltr" style="line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;">[size= 11pt; font-family: Arial,sans-serif; color: #434343; background-color: transparent; font-weight: bold; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap]The key steps in applying for [/size][size= 11pt; font-family: Arial,sans-serif; color: #1155cc; background-color: transparent; font-weight: bold; font-style: normal; font-variant: normal; text-decoration: underline; -webkit-text-decoration-skip: none; text-decoration-skip-ink: none; vertical-align: baseline; white-space: pre-wrap]CDSCO registration[/size][size= 11pt; font-family: Arial,sans-serif; color: #434343; background-color: transparent; font-weight: bold; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap] include identifying the classification of the medical device, preparing necessary documents like product technical details, ISO certifications, and clinical data. Submit the application through the Sugam portal, providing manufacturer details, device specifications, and intended use. After submission, the CDSCO reviews the application, may request additional information, and conducts an evaluation. Upon successful review, the registration certificate is issued, allowing the product to be marketed in India.[/size]