CRP FIA Test - India CDSCO Medical Device Registration

CRP FIA Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000021_9eb4930117dc2964b950df24d820a0bb_1f129c499b7b60a5796bf1d24a1605a8. This device is marketed under the brand name Multigene-Multiplex Single tube format. The license holder is Mylab Discovery S0lutions Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.

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CDSCO Registered

Class Class C

CRP FIA Test

UID: MFG/IVD/2020/000021_9eb4930117dc2964b950df24d820a0bb_1f129c499b7b60a5796bf1d24a1605a8

Brand Name

Multigene-Multiplex Single tube format

License Holder

Mylab Discovery S0lutions Pvt. Ltd

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

CRP FIA Test is an in vitro diagnostic test to be used to measure CRP concentration in human serum, plasma, and whole blood specimens. The measurement of CRP provides information for the detection and evaluation of infection, tissue injury, inflammatory disorders, and associated diseases. For professional use only

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CMV Quantitative PCR Kit

Brand: Multigene-Multiplex Single tube format

Mylab Discovery S0lutions Pvt. Ltd

CRP FIA Test - India CDSCO Medical Device Registration

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License Holder

Device Class

Approving Authority

Product Information

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