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HOMOCYSTEINE liquiUV HumaStar 600 - India CDSCO Medical Device Registration

HOMOCYSTEINE liquiUV HumaStar 600 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_6d99e9941dda4bf5cb5bec115d528616_414e52d7e8d5c53288469eece3922e7e. This device is marketed under the brand name T. The license holder is Stedman Pharmaceuticals Pvt. Ltd., and it is classified as Device Class Class B. 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 B
HOMOCYSTEINE liquiUV HumaStar 600
UID: IMP/IVD/2019/000206_6d99e9941dda4bf5cb5bec115d528616_414e52d7e8d5c53288469eece3922e7e

Brand Name

T

Device Class

Class B

Approving Authority

CDSCO

Product Information

Enzymatic UV test for the quantitative determination of homocysteine in human serum and plasma on HumaStar 300 SR and HumaStar 600

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