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CDSCO UID MFG/MD/2023/000313_c176d35b9ee6b7c34d7291e43ea408cc_4e72a4b00afabc82713d7c253727f1e7

Patient Monitoring device

NEUROSYNAPTIC COMMUNICATIONS PVT. LTD.·Device Class Class B·India CDSCO·Brand: ReMeDi
Registration details
UID
MFG/MD/2023/000313_c176d35b9ee6b7c34d7291e43ea408cc_4e72a4b00afabc82713d7c253727f1e7
Device class
Class B
Brand name
ReMeDi
License holder
NEUROSYNAPTIC COMMUNICATIONS PVT. LTD.
Approving authority
Karnataka
Product information
ReMeDi® 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
Similar products (2)
Other products with the same name or brand
Stethoscope
Brand: ReMeDi
NEUROSYNAPTIC COMMUNICATIONS PVT. LTD.
Class B
Spirometer
Brand: ReMeDi
NEUROSYNAPTIC COMMUNICATIONS PVT. LTD.
Class B
Other products from NEUROSYNAPTIC COMMUNICATIONS PVT. LTD.
Products from the same license holder (2 products)
Stethoscope
Brand: ReMeDi
Class B
Spirometer
Brand: ReMeDi
Class B
About this record

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.

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