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Malaria Pf/Pv Rapid Diagnostic test kit - India CDSCO Medical Device Registration

Malaria Pf/Pv Rapid Diagnostic test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000152_9b4dae9c32b23bbf7c7d85a6a76bd22c_b746a021fd7c3bb76ce6803952c8dfdc. The license holder is Levram Lifesciences Private 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
Malaria Pf/Pv Rapid Diagnostic test kit
UID: MFG/IVD/2022/000152_9b4dae9c32b23bbf7c7d85a6a76bd22c_b746a021fd7c3bb76ce6803952c8dfdc

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Malaria Pf/Pv Rapid diagnostic test is use for the detection of infection by Plasmodium falciparum and plasmodium vivax from whole blood

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