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NT-proBNP Test - India CDSCO Medical Device Registration

NT-proBNP Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000413_b87e2ae445318ba3e53e6a4dd4ab04a2_1e68100ba6ef6afdd36437a79f276721. This device is marketed under the brand name Finecare cTn I/CK-MB/Myo Rapid Quantitative Test. The license holder is Star Biomed Pvt. Ltd., 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.

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CDSCO Registered
Class Class C
NT-proBNP Test
UID: IMP/IVD/2021/000413_b87e2ae445318ba3e53e6a4dd4ab04a2_1e68100ba6ef6afdd36437a79f276721

Brand Name

Finecare cTn I/CK-MB/Myo Rapid Quantitative Test

License Holder

Star Biomed Pvt. Ltd.

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Finecareโ„ข NT-proBNP Rapid Quantitative Test is a fluorescence immunoassay used along with Finecareโ„ข FIA System (Finecare cTn I/CK-MB/Myo Rapid Quantitative Test) for quantitative determination of N-terminal prohormone of brain natriuretic peptide (Finecare cTn I/CK-MB/Myo Rapid Quantitative Test) in human whole blood, serum or plasma

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