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ReDS Pro System - India CDSCO Medical Device Registration

ReDS Pro System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000662_3f025678f329e6c590104c72bc91529e_8caec68646c083c93537130d04dbbb34. This device is marketed under the brand name ReDS Pro System. The license holder is M/s. Terumo India Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
ReDS Pro System
UID: IMP/MD/2022/000662_3f025678f329e6c590104c72bc91529e_8caec68646c083c93537130d04dbbb34

Brand Name

ReDS Pro System

Device Class

Class B

Approving Authority

CDSCO

Product Information

ReDS Pro is intended for use by qualified healthcare practitioners, under the direction of a physician, in hospitals, hospital-type facilities and home environments, for the non invasive monitoring and management of patients with fluid management problems in a variety of medically accepted clinical applications. The ReDS Pro System is indicated for patients: o With fluid management problems. o Taking diuretic medication. o Living with heart failure. Recovering from a coronary artery disease-related event

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