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FBI(Fibrinogen Reagent Kit ) - India CDSCO Medical Device Registration

FBI(Fibrinogen Reagent Kit ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000191_de7c545c2c6bd6bf691076f93b1e77ca_499a6ddcdb6ae926731f3e3c836dcb3f. This device is marketed under the brand name Finecare. The license holder is Matrix Labs, and it is classified as Device Class Class C. 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 C
FBI(Fibrinogen Reagent Kit )
UID: IMP/IVD/2019/000191_de7c545c2c6bd6bf691076f93b1e77ca_499a6ddcdb6ae926731f3e3c836dcb3f

Brand Name

Finecare

License Holder

Matrix Labs

Device Class

Class C

Approving Authority

CDSCO

Product Information

Quantitative measurement of fibrinogen in citrated venous whole blood

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