Anti-Cyclic Citrullinated Peptide ELISA Test Kit - India CDSCO Medical Device Registration
Anti-Cyclic Citrullinated Peptide ELISA Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000073_f5b3b926a29aae4cf199b2e65088ff00_628b7e12a077b2d60d435e649925e408. The license holder is Weldon Biotech India Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttarakhand.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
License Holder
Weldon Biotech India Pvt. Ltd.Device Class
Approving Authority
Uttarakhand
Product Information
CCP ELISA Test kit applies with indirect method. The Citrullinated peptide (NA) are coated on the micro well plates, add standards or samples into the Microwells, if there is specific antibodies in the sample, it will bind the antigen in the microwells. After thorough washing, add anti-human IgG labeled with horseradish peroxidase (NA), there will generate compounds of antigen-antibody-anti-human IgG-HRP, after thoroughly washed, add Chromogenic Reagent, and detect the OD value. Then can calculate the concentration of Anti-CCP in the sample according to the standard curve
