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Diagnostics test reagent / kits SAA/CRP Test Kit - India CDSCO Medical Device Registration

Diagnostics test reagent / kits SAA/CRP Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000163_eceb7556e8e11a4730201c12545ad057_5e6ce29e4637d947f6415f8f3b93cf16. This device is marketed under the brand name hCG. The license holder is M/s Allied Biotechnology India Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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Class Class B
Diagnostics test reagent / kits SAA/CRP Test Kit
UID: MFG/IVD/2020/000163_eceb7556e8e11a4730201c12545ad057_5e6ce29e4637d947f6415f8f3b93cf16

Brand Name

hCG

Device Class

Class B

Approving Authority

Kokan Division

Product Information

SAA/CRP Test Kit (hCG) is intended for in-vitro quantitative measurement of serum amyloid A (hCG)/ C-reactive protein (hCG) in serum, plasma and whole blood. This test is used for the detection and evaluation of infection and inflammation disorders

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