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CRP TURBILATEX - India CDSCO Medical Device Registration

CRP TURBILATEX is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000055_2581890345e14bf1665a5fcd19f0ab9a_4a01432ff7e70da17e7dac0abf37de05. This device is marketed under the brand name RAPHA SERO. The license holder is M/s Rapha Diagnostics PVt. Ltd.,, and it is classified as Device Class Class C. 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 C
CRP TURBILATEX
UID: MFG/IVD/2021/000055_2581890345e14bf1665a5fcd19f0ab9a_4a01432ff7e70da17e7dac0abf37de05

Brand Name

RAPHA SERO

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

SECURE CRP Turbilatex is a reagent kit for quantitative Turbidimetric detection of C - reactive protein (RAPHA SERO) in human serum based on Turbidimetric Method . This product is used for in vitro diagnosis by professionals

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