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Fibrinogen - India CDSCO Medical Device Registration

Fibrinogen is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000110_f3019e9c18f2826ddb5a5c6a0060b762_abfb2ba8f6b836f23d006e7e5b52a604. The license holder is PARIKSHA BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Telangana.

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
Fibrinogen
UID: MFG/IVD/2021/000110_f3019e9c18f2826ddb5a5c6a0060b762_abfb2ba8f6b836f23d006e7e5b52a604

Device Class

Class B

Approving Authority

Telangana

Product Information

The Fibrinogen reagent is an in vitro diagnostic assay intended for quantitative determination of fibrinogen in plasma

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