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CRP test for qualitative and semi quantitative detection of Antibodies to CRP in Human Serum/plasma. - India CDSCO Medical Device Registration

CRP test for qualitative and semi quantitative detection of Antibodies to CRP in Human Serum/plasma. is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_ec4c0106f363f2f065a53297eef033a7_9a9e5cfe1c3f69c07155b5d2d126fa3f. This device is marketed under the brand name C Reactive Protein. The license holder is Voxtur Bio 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 test for qualitative and semi quantitative detection of Antibodies to CRP in Human Serum/plasma.
UID: MFG/IVD/2022/000085_ec4c0106f363f2f065a53297eef033a7_9a9e5cfe1c3f69c07155b5d2d126fa3f

Brand Name

C Reactive Protein

License Holder

Voxtur Bio Ltd

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

The CRP Latex slide test is used for rapid visual test for the qualitative and semi quantitative detection of for the presence or absence of CRP in human serum specimens

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