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M-30 CFL Lyse - India CDSCO Medical Device Registration

M-30 CFL Lyse is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2018/000018_e6325e4bf4f00d14562b6b23cf3e47c1_cd8ff0cc0e702ea2cf7c29f30f40f259. This device is marketed under the brand name M-52 D diluent. The license holder is M/s Avantor Performance Materials India 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
M-30 CFL Lyse
UID: IMP/IVD/2018/000018_e6325e4bf4f00d14562b6b23cf3e47c1_cd8ff0cc0e702ea2cf7c29f30f40f259

Brand Name

M-52 D diluent

Device Class

Class B

Approving Authority

CDSCO

Product Information

For use on Mindray three part differential hematology Analyzer For use as a cyanide free lytic reagent for quantitatively determining hemoglobin and for counting and sizing leukocytes

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