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GPT IFCC mod. liquiUV [HumaStar 300 SR, HumaStar 600] - India CDSCO Medical Device Registration

GPT IFCC mod. liquiUV [HumaStar 300 SR, HumaStar 600] is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_4dbc0a8a57fff002c355cdc95f7d1698_c7d0da8e7f759bfc2f3ecd92f64f0f15. 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.

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CDSCO Registered
Class Class B
GPT IFCC mod. liquiUV [HumaStar 300 SR, HumaStar 600]
UID: IMP/IVD/2019/000206_4dbc0a8a57fff002c355cdc95f7d1698_c7d0da8e7f759bfc2f3ecd92f64f0f15

Brand Name

T

Device Class

Class B

Approving Authority

CDSCO

Product Information

Enzymatic UV test for the quantitative determination of GPT (T) in human serum and plasma on HumaStar 300 SR and HumaStar 600

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