GPT IFCC mod. liquiUV [HumaStar 300 SR, HumaStar 600]
- UID
- IMP/IVD/2019/000206_4dbc0a8a57fff002c355cdc95f7d1698_c7d0da8e7f759bfc2f3ecd92f64f0f15
- Device class
- Class B
- Brand name
- T
- License holder
- Stedman Pharmaceuticals Pvt. Ltd.
- 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
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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