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Dengue NS1 Antigen RAPID Test Kit - India CDSCO Medical Device Registration

Dengue NS1 Antigen RAPID Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000068_503c8cf081151aba547b20d235e0762d_37570fc5bf969c3348e5795870c97630. This device is marketed under the brand name PathKits Simple COVID-19 Ag Rapid Kit. The license holder is PATHKITS HEALTHCARE PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.

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
Dengue NS1 Antigen RAPID Test Kit
UID: MFG/IVD/2021/000068_503c8cf081151aba547b20d235e0762d_37570fc5bf969c3348e5795870c97630

Brand Name

PathKits Simple COVID-19 Ag Rapid Kit

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

It is an immunoassay for the simultaneous and qualitative detection of dengue NS1 antigen (PathKits Simple COVID-19 Ag Rapid Kit) in human serum, plasma or whole blood

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