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LumiraDx D-Dimer Liquid Control Solution - India CDSCO Medical Device Registration

LumiraDx D-Dimer Liquid Control Solution is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000449_99318e3065becc3369852519dd025785_47c9bc2bef15bcbae1f5a6584cb4b933. This device is marketed under the brand name LumiraDx CRP. The license holder is M/s Parekh Integrated Services Pvt. Ltd., and it is classified as Device Class Class C. 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 C
LumiraDx D-Dimer Liquid Control Solution
UID: IMP/IVD/2021/000449_99318e3065becc3369852519dd025785_47c9bc2bef15bcbae1f5a6584cb4b933

Brand Name

LumiraDx CRP

Device Class

Class C

Approving Authority

CDSCO

Product Information

The LumiraDx D-Dimer Quality Controls are intended for liquid quality control testing performed on the LumiraDx Instrument when used with the LumiraDx D-Dimer Test Strip. The Quality Controls provide users with assurance that the device is performing within specification

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