Brucella Ab Rapid Test - India CDSCO Medical Device Registration
Brucella Ab Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000078_e2718310f58f0a13869c42c117159750_940b1940528dd1ea8cc48e9097bc9058. This device is marketed under the brand name IgG and IgM. The license holder is Dia Sure Immunodiagnostic LLP, and it is classified as Device Class Class B. The approving authority is South Delhi Division.
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Brand Name
IgG and IgM
License Holder
Dia Sure Immunodiagnostic LLPDevice Class
Approving Authority
South Delhi Division
Product Information
for detection of Brucella Antibody in plasma, serum of cattle, sheep, goat or raw milk samples
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