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NT-proBNP Fast Test Kit - India CDSCO Medical Device Registration

NT-proBNP Fast Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000410_580cb484c1bde95053451e8e8c06b28c_abe63d35fdf73e4cac1ae4f8d7b8bf22. This device is marketed under the brand name Imumunofluorescence Assay. The license holder is Vector Biotek 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 Fast Test Kit
UID: IMP/IVD/2019/000410_580cb484c1bde95053451e8e8c06b28c_abe63d35fdf73e4cac1ae4f8d7b8bf22

Brand Name

Imumunofluorescence Assay

License Holder

Vector Biotek Pvt Ltd

Device Class

Class C

Approving Authority

CDSCO

Product Information

NT-proBNP Fast Test Kit (Imumunofluorescence Assay) is intended for in vitro quantitative determination of N-terminal B-type natriuretic peptide precursor (Imumunofluorescence Assay) in serum, plasma or whole blood. This test is used as an aid in the clinical diagnosis, prognosis and evaluation of Heart Failure (Imumunofluorescence Assay)

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