Fibrinogen Reagent Kit - India CDSCO Medical Device Registration

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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CDSCO Registered

Class Class C

Fibrinogen Reagent Kit

UID: IMP/IVD/2020/000278_1c93a1c39e80fdf566a23e14a414f92b_f5f00392427df42abdec5abc3b8d8719

Brand Name

CEA

License Holder

RAPID DIAGNOSTIC PVT. LTD.

Device Class

Class C

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