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Beta hCG FIA Test - India CDSCO Medical Device Registration

Beta hCG FIA Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000062_6e91ca48ceca494c16bcb91d15da5890_8faf9fc85a409847974651b2e43acf44. 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
Beta hCG FIA Test
UID: MFG/IVD/2021/000062_6e91ca48ceca494c16bcb91d15da5890_8faf9fc85a409847974651b2e43acf44

Brand Name

hCG

Device Class

Class B

Approving Authority

Pune Division

Product Information

Beta hCG FIA Test is a fluorescence immunoassay for the determination of total Beta hCG levels in a human specimen using FIA Analyzers. This test is an in vitro diagnostic use test and is intended for professional testing and use as an aid in the early detection of pregnancy. More specific alternative diagnosis methods should be performed to obtain confirmation of pregnancy

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