Immunoglobulin E Antibody Test - India CDSCO Medical Device Registration
Immunoglobulin E Antibody Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000103_f47f86cfcf37307d5599fa3b038fe65b_16a3a0eb138d3bf697a2f204d3ce4193. This device is marketed under the brand name RF-IgM. The license holder is Genovik Biotech Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Rajasthan.
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Brand Name
RF-IgM
License Holder
Genovik Biotech Pvt. Ltd.Device Class
Approving Authority
Rajasthan
Product Information
Genovik Immunoglobulin E (RF-IgM) Antibody Test is a lateral flow chromatographic immunoassay for the qualitative detection of human IgE antibody in whole blood, serum or plasma to aid in the diagnosis of allergy
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ESTRADIOL Test
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Anti-Cyclic Citrullinated Peptide Test
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FILARIASIS Antibody Test
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Glycosylated hemoglobin Test
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Free Triiodothyronine Test
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