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Creatinine liquicolor HumaStar 600 - India CDSCO Medical Device Registration

Creatinine liquicolor HumaStar 600 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_b169367a48b4d7ddf3556a6ecf92d341_19880306a8d0efbcef64dc6db08c0e40. 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
Creatinine liquicolor HumaStar 600
UID: IMP/IVD/2019/000206_b169367a48b4d7ddf3556a6ecf92d341_19880306a8d0efbcef64dc6db08c0e40

Brand Name

T

Device Class

Class B

Approving Authority

CDSCO

Product Information

Enzymatic assay for the quantitative determination of creatinine in human serum on HumaStar 300SR and HumaStar 600

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