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Alinity c Direct Bilirubin Reagent Kit - India CDSCO Medical Device Registration

Alinity c Direct Bilirubin Reagent Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2018/000029_fdd3b20a09c713f482c4f46c7b88f556_2e6e3a101b7a4f85110266ce58f27cfa. This device is marketed under the brand name Alinity c Ultra HDL Reagent Kit. The license holder is Abbott Healthcare 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
Alinity c Direct Bilirubin Reagent Kit
UID: IMP/IVD/2018/000029_fdd3b20a09c713f482c4f46c7b88f556_2e6e3a101b7a4f85110266ce58f27cfa

Brand Name

Alinity c Ultra HDL Reagent Kit

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Alinity c Direct Bilirubin assay is used for the quantitative analysis of direct bilirubin in human serum or plasma on the Alinity c analyzer

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