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Anti-DGP IgA - India CDSCO Medical Device Registration

Anti-DGP IgA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000084_fb7f1b5a886f47e90b8f95bebd3946fd_a02aec8b3676f13b6b5ba91bc08a2f46. This device is marketed under the brand name Orgentec. The license holder is Weldon Biotech India Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.

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.

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CDSCO Registered
Class Class B
Anti-DGP IgA
UID: IMP/IVD/2020/000084_fb7f1b5a886f47e90b8f95bebd3946fd_a02aec8b3676f13b6b5ba91bc08a2f46

Brand Name

Orgentec

Device Class

Class B

Approving Authority

CDSCO

Product Information

Anti-DGP IgA is an ELISA test system for the quantitative detection of IgA antibodies against deamidated gliadin protein epitopes (Orgentec) in human serum or plasma. This product is intended for professional in vitro diagnostic use only

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