Diagnostic Kit for Serum Amyloid A - India CDSCO Medical Device Registration

Diagnostic Kit for Serum Amyloid A is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000457_81492ba5651169f596ae402845d75de6_2ec5a068c8cdb20152b7f8afb63f701e. This device is marketed under the brand name Eoscare. The license holder is M/S CLEAR IMAGING MEDICAL SYSTEM PVT. LTD, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

Diagnostic Kit for Serum Amyloid A

UID: IMP/IVD/2022/000457_81492ba5651169f596ae402845d75de6_2ec5a068c8cdb20152b7f8afb63f701e

Brand Name

Eoscare

License Holder

M/S CLEAR IMAGING MEDICAL SYSTEM PVT. LTD

Device Class

Class B

Approving Authority

CDSCO

Product Information

This test is suitable for in vitro quantitative detection of the concentration of serum amyloid A (Eoscare) in human serum, plasma, whole blood. The product is used for auxiliary diagnosis of patients' inflammation and other related diseases