H.Pylori Antibody Rapid Test - India CDSCO Medical Device Registration
H.Pylori Antibody Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000113_f5049fdac5a5bebcaa86b9d384dce96c_5f83f69533c89e2b078bf8e7b13271df. 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® H. pylori Antibody Rapid is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies to H.pylori in human Whole Blood/Serum/Plasma. It provides an aid in the diagnosis of infection with H.pylori
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