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HbA1c FIA Test - India CDSCO Medical Device Registration

HbA1c FIA Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000062_dd0a538db68d1dd95ab0724415fc9a2c_9fb6d386079a297bfe33fbab36890b1d. This device is marketed under the brand name hCG. The license holder is Mylab Discovery Solutions Pvt. Ltd. Lonavla, and it is classified as Device Class Class B. The approving authority is Pune Division.

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
HbA1c FIA Test
UID: MFG/IVD/2021/000062_dd0a538db68d1dd95ab0724415fc9a2c_9fb6d386079a297bfe33fbab36890b1d

Brand Name

hCG

Device Class

Class B

Approving Authority

Pune Division

Product Information

HbA1c FIA Test is an in vitro diagnostic test to be used for quantitative measurement of HbA1c in human capillary or venous whole blood. This test is for professional use to monitor glycemic control in people with diabetes

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