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Beta-HCG Test - India CDSCO Medical Device Registration

Beta-HCG Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000413_749f0ccebf045c1f5c45756ce666391b_03097c471d624ea47c7f983868569d7f. This device is marketed under the brand name Finecare Beta-HCG Rapid Quantitative Test. The license holder is Star Biomed Pvt. 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
Beta-HCG Test
UID: IMP/IVD/2021/000413_749f0ccebf045c1f5c45756ce666391b_03097c471d624ea47c7f983868569d7f

Brand Name

Finecare Beta-HCG Rapid Quantitative Test

License Holder

Star Biomed Pvt. Ltd.

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Finecareโ„ข ฮฒ-hCG Rapid Quantitative Test is a fluorescence immunoassay used along with Finecareโ„ข FIA System (Finecare Beta-HCG Rapid Quantitative Test) for quantitative determination of ฮฒ-hCG in human whole blood, serum or plasma

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