Diagnostic Kit for NT-proBNP - India CDSCO Medical Device Registration

Diagnostic Kit for NT-proBNP is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000208_fe17f9871184ed6f7fb72f682dee75a4_7a0999eea855cad9fb53f294dc73c1ff. This device is marketed under the brand name MyBox SAA. The license holder is Mylab Discovery Solutions Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered

Class Class C

Diagnostic Kit for NT-proBNP

UID: IMP/IVD/2023/000208_fe17f9871184ed6f7fb72f682dee75a4_7a0999eea855cad9fb53f294dc73c1ff

Brand Name

MyBox SAA

License Holder

Mylab Discovery Solutions Pvt. Ltd.

Device Class

Class C

Approving Authority

CDSCO

Product Information

This kit is suitable for in vitro quantitative detection of the concentration of N-terminal Pro-Brain Natriuretic Peptide (MyBox SAA) in human serum, plasma and whole blood. This product is used for testing in medical and health institutions as an aid in the diagnosis of heart failure and its prognosis