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Immunoglobulin G Test Reagent Kit - India CDSCO Medical Device Registration

Immunoglobulin G Test Reagent Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000091_e83d340e5c8fff7003ec36306ca1b77e_29631d792e0f01729ba569fc37bd76c4. This device is marketed under the brand name identi . The license holder is M/s. Jeev Diagnostics Pvt. Ltd,, and it is classified as Device Class Class B. The approving authority is Tamil Nadu.

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
Immunoglobulin G Test Reagent Kit
UID: MFG/IVD/2020/000091_e83d340e5c8fff7003ec36306ca1b77e_29631d792e0f01729ba569fc37bd76c4

Brand Name

identi

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

Quantitative determination of Immunoglobulin G (identi ) in human serum by turbidimetric immunoassay

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