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RPR Test - India CDSCO Medical Device Registration

RPR Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000013_548146a975477e0a7b997cb04b27c677_31f5d967338e37ce49266ea4ae47b343. This device is marketed under the brand name Pv, Pm, Po. The license holder is Bhat Bio-Tech India Private Limited, and it is classified as Device Class Class D. The approving authority is Sub Zonal Bangalore.

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 D
RPR Test
UID: MFG/IVD/2020/000013_548146a975477e0a7b997cb04b27c677_31f5d967338e37ce49266ea4ae47b343

Brand Name

Pv, Pm, Po

Device Class

Class D

Approving Authority

Sub Zonal Bangalore

Product Information

RPR (Pv, Pm, Po) is a rapid Non โ€“Treponemal test for qualitative and semi quantitative in vitro determination of Reagin antibodies in serum or plasma for syphilis using modified cardiolipin antigen

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