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Dengue/Chikungunya PCR Detection Kit - India CDSCO Medical Device Registration

Dengue/Chikungunya PCR Detection Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2018/000002_d6d239b9a43ca9e449e612a5fc7e505b_5b7715a091ce4c1ca27c3efcb2134eb0. This device is marketed under the brand name TRUPCR® MPN Panel Kit. The license holder is KILPEST INDIA LIMITED, 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
Dengue/Chikungunya PCR Detection Kit
UID: MFG/IVD/2018/000002_d6d239b9a43ca9e449e612a5fc7e505b_5b7715a091ce4c1ca27c3efcb2134eb0

Brand Name

TRUPCR® MPN Panel Kit

License Holder

KILPEST INDIA LIMITED

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

TRUPCR® Dengue/Chikungunya Detection Kit is an in vitro nucleic acid amplification assay for the qualitative detection and differentiation of Dengue virus RNA and Chikungunya virus RNA in human serum or plasma (TRUPCR® MPN Panel Kit) specimens using Real Time PCR method. The results from the TRUPCR® Dengue/Chikungunya Detection Kit must be interpreted within the context of all relevant clinical and laboratory findings. An endogenous internal control has been integrated into the kit in order to check extraction and PCR inhibition

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