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CDSCO UID MFG/IVD/2022/000029_f9c3b9c6dd98d5ed6dfb34100e61bd16_c0bda067a055b545fb487da8a7e53ede

Quantitative Turbidimetric Immunoassay for CRP

CORAL CLINICAL SYSTEMS A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED·Device Class Class B·India CDSCO·Brand: SEROQUANT FERRITIN LEVEL I
Registration details
UID
MFG/IVD/2022/000029_f9c3b9c6dd98d5ed6dfb34100e61bd16_c0bda067a055b545fb487da8a7e53ede
Device class
Class B
Brand name
SEROQUANT FERRITIN LEVEL I
License holder
CORAL CLINICAL SYSTEMS A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED
Approving authority
Goa
Product information
Quantia CRP 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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About this record

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_c0bda067a055b545fb487da8a7e53ede. 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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