ELISA Kit for detection of IgM antibodies to Toxoplasma in Human serum/plasma - India CDSCO Medical Device Registration
ELISA Kit for detection of IgM antibodies to Toxoplasma in Human serum/plasma is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000068_a06ca5ba4778ae274b6fb5cc6a54c686_b3e7c2e7d4eb725f8b1f3f2dd86c7ade. This device is marketed under the brand name Cassette format. The license holder is Biogenix Inc. Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.
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Brand Name
Cassette format
License Holder
Biogenix Inc. Pvt. Ltd.Device Class
Approving Authority
CDSCO -North Zone, Ghaziabad
Product Information
A Toxoplasma gondii test of ToRCH & reagents/kits is a medical device other intended for the detection of infectious Toxoplasma gondii in serum/body agents fluids
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