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FER Rapid Quantitative Test - India CDSCO Medical Device Registration

FER Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000074_c8bdf72a46fe0a97ed464f2507d23c1d_d72802b632a3912ff68636f732391d97. This device is marketed under the brand name Glycated Hemoglobin. The license holder is FINOVA HEALTHCARE 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
FER Rapid Quantitative Test
UID: IMP/IVD/2022/000074_c8bdf72a46fe0a97ed464f2507d23c1d_d72802b632a3912ff68636f732391d97

Brand Name

Glycated Hemoglobin

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Ferritin Rapid Quantitative Test along with Aehealth FIA Meter is intended for vitro quantitative determination of Ferritin in human whole blood, serum or plasma

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