CDSCO UID IMP/IVD/2020/000278_1c93a1c39e80fdf566a23e14a414f92b_f5f00392427df42abdec5abc3b8d8719

Fibrinogen Reagent Kit

RAPID DIAGNOSTIC PVT. LTD.·Device Class Class C·India CDSCO·Brand: CEA

Registration details

UID: IMP/IVD/2020/000278_1c93a1c39e80fdf566a23e14a414f92b_f5f00392427df42abdec5abc3b8d8719
Device class: Class C
Brand name: CEA
License holder: RAPID DIAGNOSTIC PVT. LTD.
Approving authority: CDSCO
Product information: The Fibrinogen Reagent Kit (CEA) is used along with Optical Coagulation Analyzer (CEA) for quantitative measurement of fibrinogen in citrated venous whole blood

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About this record

Fibrinogen Reagent Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000278_1c93a1c39e80fdf566a23e14a414f92b_f5f00392427df42abdec5abc3b8d8719. This device is marketed under the brand name CEA. The license holder is RAPID DIAGNOSTIC PVT. LTD., and it is classified as Device Class Class C. The approving authority is CDSCO.

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