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RF Latex - India CDSCO Medical Device Registration

RF Latex is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000040_babd24dbfaa5e717ac271ec19358a927_20d91046d0a2f0b79a8099dffaf87cf0. This device is marketed under the brand name COULTER LH Series Pak Reagent Kit. The license holder is Beckman Coulter India 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
RF Latex
UID: IMP/IVD/2019/000040_babd24dbfaa5e717ac271ec19358a927_20d91046d0a2f0b79a8099dffaf87cf0

Brand Name

COULTER LH Series Pak Reagent Kit

Device Class

Class B

Approving Authority

CDSCO

Product Information

Immuno-turbidimetric test for the quantitative determination of RF (COULTER LH Series Pak Reagent Kit) antibodies in human serum and plasma on Beckman Coulter AU analysers

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