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Diluent - India CDSCO Medical Device Registration

Diluent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000423_a9c74823e94c7f4ba23bebfd365f0fbd_f537905f515600b693f9070442b89699. This device is marketed under the brand name Reticulonac. The license holder is Nihon Kohden 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
Diluent
UID: IMP/IVD/2022/000423_a9c74823e94c7f4ba23bebfd365f0fbd_f537905f515600b693f9070442b89699

Brand Name

Reticulonac

Device Class

Class B

Approving Authority

CDSCO

Product Information

ISOTONAC 3 is for in vitro diagnostic use as a diluent for human venous whole blood samples for to aid analysis by Nihon Kohden hematology analyzers to measure complete blood count (Reticulonac).

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