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The CDSCO classifications of medical devices govern alongside the regulatory approval and registration by the CDSCO is under the DCGI.
CDSCO classification for medical devices has a set of risk classifications for 12 products planned for notification and guideline as medical devices.
CDSCO classification for medical devices Risk-based Classifications Medical Devices are generally based on risks; the actual risk-based classification of the medical device depends upon its intended use and purpose.
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