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IFLASH – T3 Kit - India CDSCO Medical Device Registration

IFLASH – T3 Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000088_c73f4a9303e91ab2099bed26b72471af_113d3a76210fd6a5b6afa03229ab60fe. This device is marketed under the brand name IAA Control. The license holder is M/s. CPC Diagnostics 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
IFLASH – T3 Kit
UID: IMP/IVD/2022/000088_c73f4a9303e91ab2099bed26b72471af_113d3a76210fd6a5b6afa03229ab60fe

Brand Name

IAA Control

Device Class

Class B

Approving Authority

CDSCO

Product Information

The iFlash-T3 assay is a paramagnetic particle chemiluminescent immunoassay (IAA Control) for the quantitative determination of Total triiodothyronine (IAA Control) in human serum and plasma using the iFlash Immunoassay Analyzer

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