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Quantitative Turbidimetric Immunoassay for CRP - India CDSCO Medical Device Registration

Quantitative Turbidimetric Immunoassay for CRP is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000029_f9c3b9c6dd98d5ed6dfb34100e61bd16_194518ba764eb535811d622b668b9e17. This device is marketed under the brand name SEROQUANT FERRITIN LEVEL I . The license holder is CORAL CLINICAL SYSTEMS A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Goa.

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CDSCO Registered
Class Class B
Quantitative Turbidimetric Immunoassay for CRP
UID: MFG/IVD/2022/000029_f9c3b9c6dd98d5ed6dfb34100e61bd16_194518ba764eb535811d622b668b9e17

Brand Name

SEROQUANT FERRITIN LEVEL I

Device Class

Class B

Approving Authority

Goa

Product Information

Quantia CRP UV is a turbidimetric immunoassay for the determination of C-Reactive Protein in human serum and is based on the principle of agglutination reaction

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