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DILUENT/SHEATH - India CDSCO Medical Device Registration

DILUENT/SHEATH is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000075_c20a0a93831ecb9597d7fddf6d90d799_629fdbf39727c854ff119bcab71821a3. This device is marketed under the brand name WBC Reagent, PART B. 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
DILUENT/SHEATH
UID: IMP/IVD/2022/000075_c20a0a93831ecb9597d7fddf6d90d799_629fdbf39727c854ff119bcab71821a3

Brand Name

WBC Reagent, PART B

Device Class

Class B

Approving Authority

CDSCO

Product Information

Prepares each cell for counting and sizing, acting as the primary diluting fluid for the RBC/PLT and RETC. Act as the diluent for the RBCs, PLTs, and hemoglobin

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