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Biolatex®RF (CRM®Diagnostic Systems RF ) - India CDSCO Medical Device Registration

Biolatex®RF (CRM®Diagnostic Systems RF ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000337_35774219c82052f871b4148a6e5310d6_b1bb35349ec0f10fcecddf350a3ead1a. This device is marketed under the brand name CRM®Diagnostic Systems Cystatin C. The license holder is SIRUS BIOCARE PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is CDSCO.

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 B
Biolatex®RF (CRM®Diagnostic Systems RF )
UID: IMP/IVD/2019/000337_35774219c82052f871b4148a6e5310d6_b1bb35349ec0f10fcecddf350a3ead1a

Brand Name

CRM®Diagnostic Systems Cystatin C

Device Class

Class B

Approving Authority

CDSCO

Product Information

Diagnostic reagent for quantitative in vitro determination of RF in human serum on photometric systems

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