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RPR SYPHILIS SCREENING TEST Kit/Device - India CDSCO Medical Device Registration

RPR SYPHILIS SCREENING TEST Kit/Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000009_2e579d92ea797727d744e95b57e46777_4717e7cc0558135c3009e0e4b05483f4. The license holder is Sidak Lifecare Pvt Ltd, and it is classified as Device Class Class D. 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 D
RPR SYPHILIS SCREENING TEST Kit/Device
UID: MFG/IVD/2021/000009_2e579d92ea797727d744e95b57e46777_4717e7cc0558135c3009e0e4b05483f4

Device Class

Class D

Approving Authority

Sub Zonal Baddi

Product Information

For detection of syphilis in human blood/plasma

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