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/2023/000091_7caa6965d917ec52151d2f8b3d9ad5d5_ecf44203a71e0fd23a47ea2191dec92f. This device is marketed under the brand name GeneBio. The license holder is GeneBio Healthare Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.
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Brand Name
GeneBio
License Holder
GeneBio Healthare Pvt LtdDevice Class
Approving Authority
Uttar Pradesh
Product Information
H. Pylori Antibody Rapid Test is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of antibodies (GeneBio) against Helicobacter pylori (GeneBio) in human serum, plasma or whole blood
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