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Alinity c Ultra HDL Reagent Kit - India CDSCO Medical Device Registration

Alinity c Ultra HDL Reagent Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2018/000029_cc3723d51160c58d2668d47e44b4ab95_5c15659677605a5fd810c2822f9c75ca. 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 Ultra HDL Reagent Kit
UID: IMP/IVD/2018/000029_cc3723d51160c58d2668d47e44b4ab95_5c15659677605a5fd810c2822f9c75ca

Brand Name

Alinity c Ultra HDL Reagent Kit

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Alinity c Ultra HDL assay is used for the quantitation of high density lipoprotein (Alinity c Ultra HDL Reagent Kit) cholesterol in human serum or plasma on the Alinity c analyzer

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