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LH Rapid Quantitative Test - India CDSCO Medical Device Registration

LH Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000039_e2155b08104291a6af4a602972eadd3d_6cee779dd28d8250c2e00ed3e8add7e4. This device is marketed under the brand name Finecare . The license holder is M/s Avantor Performance Materials India 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
LH Rapid Quantitative Test
UID: IMP/IVD/2019/000039_e2155b08104291a6af4a602972eadd3d_6cee779dd28d8250c2e00ed3e8add7e4

Brand Name

Finecare

Device Class

Class B

Approving Authority

CDSCO

Product Information

Intended for quantitative determination of Luteinizing hormone (Finecare ) in human whole blood or plasma

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