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ACTH CLIA Microparticles - India CDSCO Medical Device Registration

ACTH CLIA Microparticles is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000395_e4f4e0eee85e56c6050b52bb465a12cb_7c34f98fa1fe8ce14a96e5b4dd9df7ae. This device is marketed under the brand name T4 CLIA Microparticles. The license holder is Matrix Labs, 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
ACTH CLIA Microparticles
UID: IMP/IVD/2019/000395_e4f4e0eee85e56c6050b52bb465a12cb_7c34f98fa1fe8ce14a96e5b4dd9df7ae

Brand Name

T4 CLIA Microparticles

License Holder

Matrix Labs

Device Class

Class B

Approving Authority

CDSCO

Product Information

This assay is based on a chemiluminescent microparticle immunoassay (T4 CLIA Microparticles) for the quantitative determination of ACTH (T4 CLIA Microparticles) in human plasma (T4 CLIA Microparticles)

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