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Prolactin Test - India CDSCO Medical Device Registration

Prolactin Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000413_bb35c00e14c6318f517e926c12558a87_91240a28134c922e226f734c62fcf84d. 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
Prolactin Test
UID: IMP/IVD/2021/000413_bb35c00e14c6318f517e926c12558a87_91240a28134c922e226f734c62fcf84d

Brand Name

Finecare Beta-HCG Rapid Quantitative Test

License Holder

Star Biomed Pvt. Ltd.

Device Class

Class B

Approving Authority

CDSCO

Product Information

The FinecareTM Prolactin Rapid Quantitative Test is a fluorescence immunoassay used along with FinecareTM FIA Meters (Finecare Beta-HCG Rapid Quantitative Test) for quantitative measurement of Prolactin (Finecare Beta-HCG Rapid Quantitative Test) in human whole blood, serum or plasma

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