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LIAISON Control ACTH - India CDSCO Medical Device Registration

LIAISON Control ACTH is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000089_a027a9ae792799098629dea05ace4153_7fa747330eebf0adda321270469ebec3. This device is marketed under the brand name LIAISON® EASY System Liquid. The license holder is Diasorin Healthcare 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
LIAISON Control ACTH
UID: IMP/IVD/2019/000089_a027a9ae792799098629dea05ace4153_7fa747330eebf0adda321270469ebec3

Brand Name

LIAISON® EASY System Liquid

Device Class

Class B

Approving Authority

CDSCO

Product Information

The LIAISON® ACTH controls (LIAISON® EASY System Liquid) are to be used in LIAISON® ACTH chemiluminescent immunoassays (LIAISON® EASY System Liquid) as a means of checking reliability of assay runs. The performance characteristics of LIAISON® Control ACTH have not been established for any other assays or instrument platforms different from LIAISON® and LIAISON® XL

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