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Rapid test for detection of Antigens to Dengue NS1 in Human Serum/Plasma/Whole Blood - India CDSCO Medical Device Registration

Rapid test for detection of Antigens to Dengue NS1 in Human Serum/Plasma/Whole Blood is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_ca6c19b11338a6e10b1f0e05db27eacd_30d7df917d039f67efa365b901f6c027. 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.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class C
Rapid test for detection of Antigens to Dengue NS1 in Human Serum/Plasma/Whole Blood
UID: MFG/IVD/2022/000085_ca6c19b11338a6e10b1f0e05db27eacd_30d7df917d039f67efa365b901f6c027

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 Dengue NS1 antigen test card is used for rapid visual test for the qualitative detection of for the presence or absence of Antigens specific to Dengue NS1 in human whole blood /serum/plasma specimens

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