Pure Global

NT-proBNP Rapid Quantitative Test - India CDSCO Medical Device Registration

NT-proBNP Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000035_a763cc1c457e1862353fd53b79990d71_fcaf75f133e428b1c1514d00ffdfe6f6. This device is marketed under the brand name Biotime. The license holder is DIYA SCIENTIFIC, and it is classified as Device Class Class C. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
NT-proBNP Rapid Quantitative Test
UID: IMP/IVD/2022/000035_a763cc1c457e1862353fd53b79990d71_fcaf75f133e428b1c1514d00ffdfe6f6

Brand Name

Biotime

License Holder

DIYA SCIENTIFIC

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Biotime NT-proBNP Rapid Quantitative Test is intended to quantify the concentration of NT-proBNP in human serum, plasma or whole blood on Biotime FIA Analyzers by fluorescent immunoassay. The test is used as an aid detection of heart failure. -Fluorescent immunoassay -Heart failure For in vitro diagnostic use only. For professional use only

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name or brand