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Patient Monitoring device - India CDSCO Medical Device Registration

Patient Monitoring device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000313_c176d35b9ee6b7c34d7291e43ea408cc_4e72a4b00afabc82713d7c253727f1e7. This device is marketed under the brand name ReMeDi. The license holder is NEUROSYNAPTIC COMMUNICATIONS PVT. LTD., and it is classified as Device Class Class B. The approving authority is Karnataka.

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
Patient Monitoring device
UID: MFG/MD/2023/000313_c176d35b9ee6b7c34d7291e43ea408cc_4e72a4b00afabc82713d7c253727f1e7

Brand Name

ReMeDi

Device Class

Class B

Approving Authority

Karnataka

Product Information

ReMeDiยฎ NOVA is to be used for spot check measuring, displaying, reviewing and storing of multiple physiological parameters including Electrocardiograph (ReMeDi), Blood Oxygen Saturation (ReMeDi), Beats Per Minute (ReMeDi), Body Temperature, Non-Invasive Blood Pressure Measurement (ReMeDi) through wireless mode in home / healthcare facility environment

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