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RF DIRECT LATEX - India CDSCO Medical Device Registration

RF DIRECT LATEX is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000502_cdc48653755cc03c4edfc7c9f9ac1b48_8ac137e335ec851ee53d9d81f516d682. This device is marketed under the brand name QCA. The license holder is ARK Diagnostic System Pvt.Ltd, 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
RF DIRECT LATEX
UID: IMP/IVD/2023/000502_cdc48653755cc03c4edfc7c9f9ac1b48_8ac137e335ec851ee53d9d81f516d682

Brand Name

QCA

Device Class

Class B

Approving Authority

CDSCO

Product Information

โ€œIn vitroโ€ determination of rheumatoid factors in serum

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