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UREA liquiUV HumaStar 600 - India CDSCO Medical Device Registration

UREA liquiUV HumaStar 600 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_d1e4f313defb35335007b5f267c8384b_df4bffb55551735fad7caa11c98f8885. 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
UREA liquiUV HumaStar 600
UID: IMP/IVD/2019/000206_d1e4f313defb35335007b5f267c8384b_df4bffb55551735fad7caa11c98f8885

Device Class

Class B

Approving Authority

CDSCO

Product Information

Fully enzymatic UV test for the quantitative determination of urea in human serum or plasma on HumaStar 300 SR and HumaStar 600

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