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Dengue Combo RAPID Test Kit - India CDSCO Medical Device Registration

Dengue Combo RAPID Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000068_c7e24c9a70225aa7b9399d9b383a9163_c9712b587a04fc28f0f51c5e7887078f. 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 Combo RAPID Test Kit
UID: MFG/IVD/2021/000068_c7e24c9a70225aa7b9399d9b383a9163_c9712b587a04fc28f0f51c5e7887078f

Brand Name

PathKits Simple COVID-19 Ag Rapid Kit

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

It is a solid phase immuno chromatographic assay for the rapid, qualitative and differential detection of NS1 antigen and IgG and IgM antibodies to dengue virus (PathKits Simple COVID-19 Ag Rapid Kit) in human serum, plasma or whole blood

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