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Rheumatoid Factor IgA - India CDSCO Medical Device Registration

Rheumatoid Factor IgA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000558_ff52f65da482dc3811a51d722e8b82cb_c72d9d619e9928e3e712d397a9d8f5f0. This device is marketed under the brand name Anti-Gliadin IgG. The license holder is Sebia Diagnostics India 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
Rheumatoid Factor IgA
UID: IMP/IVD/2021/000558_ff52f65da482dc3811a51d722e8b82cb_c72d9d619e9928e3e712d397a9d8f5f0

Brand Name

Anti-Gliadin IgG

Device Class

Class B

Approving Authority

CDSCO

Product Information

Rheumatoid Factor IgA is an ELISA-based test system for the quantitative measurement of IgA class rheumatoid factor in human serum or plasma samples. This product is intended for professional in vitro diagnostic use only. The test is used as an aid in the differential diagnosis of rheumatoid arthritis (Anti-Gliadin IgG), and presence of rheumatoid factors (Anti-Gliadin IgG) is an integral part of the current ACR criteria for classification of RA. In established RA, high titres of serum IgG and especially IgM RF indicate poor prognosis. The presence of either IgG or IgA RF in patients with long-standing RA may be a prognostic indicator of systemic manifestations. Evaluation of a test result should always take into account all clinical and laboratory findings

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DJ Fang

DJ Fang

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