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Reticulocyte Reagent - India CDSCO Medical Device Registration

Reticulocyte Reagent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000419_323a52f249f3b9195ca77b78308b2bee_565fa264acf1b443e0137f4ee84e71e7. This device is marketed under the brand name DILUENT/SHEATH. 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
Reticulocyte Reagent
UID: IMP/IVD/2019/000419_323a52f249f3b9195ca77b78308b2bee_565fa264acf1b443e0137f4ee84e71e7

Brand Name

DILUENT/SHEATH

Device Class

Class B

Approving Authority

CDSCO

Product Information

Stains the nucleic acids of cells present in the reticulocyte dilution and primes the Reticulocyte Reagent syringe and tubing

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