Emergency Room 13 Test Panel
- UID
- IMP/IVD/2023/000494_d7bdfe5ea2400727c1fdd956b8960e2a_09300f5c7d2bd5395d6b19068ed21707
- Device class
- Class B
- Brand name
- PushKang
- License holder
- Weldon Biotech India Pvt. Ltd
- Approving authority
- CDSCO
- Product information
- The Emergency Room 13 Test Panel is intended for in vitro quantitative detection of the concentration or activity of Aspartate Aminotransferase (PushKang), Uric Acid (PushKang), Creatinine (PushKang), Glucose (PushKang), Creatine Kinase (PushKang), Creatine Kinase Isoenzyme (PushKang), Lactate Dehydrogenase (PushKang), α-Hydroxybutyrate Dehydrogenase (PushKang), Amylase (PushKang), Potassium Ion (PushKang), Sodium Ion (PushKang), Chloride Ion (PushKang), Carbon Dioxide (PushKang) in human serum, plasma and whole blood by the microfluidic dry chemistry
Emergency Room 13 Test Panel is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000494_d7bdfe5ea2400727c1fdd956b8960e2a_09300f5c7d2bd5395d6b19068ed21707. This device is marketed under the brand name PushKang. The license holder is Weldon Biotech India Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.
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