Typhoid IgG/IgM Antibody Rapid Test - India CDSCO Medical Device Registration
Typhoid IgG/IgM Antibody Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000113_f2f763222f8a2b1aa0036f9b23e18504_435014f9783b164a115771f335c8c59c. This device is marketed under the brand name Chimera. The license holder is CHIMERA BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is South Delhi Division.
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Brand Name
Chimera
License Holder
CHIMERA BIOTECH PRIVATE LIMITEDDevice Class
Approving Authority
South Delhi Division
Product Information
The Chimera® Typhoid IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of anti-Salmonella typhi (Chimera) IgG and IgM in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with S. typhi
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