Anti-Mullerian Hormone ELISA test Kit - India CDSCO Medical Device Registration
Anti-Mullerian Hormone ELISA test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000060_edd102b572f3fc6fc0a1f4591b33699e_a8d000c598f9801173ffe93036f633f6. This device is marketed under the brand name EIA. The license holder is Genomix Molecular Diagnostics Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.
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Brand Name
EIA
License Holder
Genomix Molecular Diagnostics Pvt LtdDevice Class
Approving Authority
Telangana
Product Information
For the quantitative measurement of AMH in human serum and plasma

