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SYPHILIS RAPID TEST KIT - India CDSCO Medical Device Registration

SYPHILIS RAPID TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000082_14b14de5d505206ab56c7774ae3964cf_c843228267119410cc33129216407e3f. The license holder is PEERLESS BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is Central Drug Standard Control Organisation, South 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 D
SYPHILIS RAPID TEST KIT
UID: MFG/IVD/2022/000082_14b14de5d505206ab56c7774ae3964cf_c843228267119410cc33129216407e3f

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

The Syphilis Rapid Test Kit is a rapid chromatographic immunoassay for the qualitative detection of antibodies ##PLACEHOLDER_0## to Treponema Pallidum ##PLACEHOLDER_0## in whole blood, serum or plasma

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