Electrolyte 7 Test Panel - India CDSCO Medical Device Registration

Electrolyte 7 Test Panel is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000494_e8801232569e7244f57e6582af6479d4_72a20e1903395a41e760b0e5adec2532. 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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CDSCO Registered

Class Class B

Electrolyte 7 Test Panel

UID: IMP/IVD/2023/000494_e8801232569e7244f57e6582af6479d4_72a20e1903395a41e760b0e5adec2532

Brand Name

PushKang

License Holder

Weldon Biotech India Pvt. Ltd

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Electrolyte 7 Test Panel is intended for in vitro quantitative detection of the concentration of Potassium Ion (PushKang), Calcium Ion (PushKang), Sodium Ion (PushKang), Chloride Ion (PushKang), Carbon Dioxide(PushKang), Magnesium Ion (PushKang), and Inorganic Phosphorus (PushKang) in human serum, plasma and whole blood by the microfluidic dry chemistry

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General Chemistry 9 Test Panel

Brand: PushKang

Weldon Biotech India Pvt. Ltd

Electrolyte 7 Test Panel - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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