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CELLPACK DFL - India CDSCO Medical Device Registration

CELLPACK DFL is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000255_8d6f74525be560685b3609a84e8770fd_afb81585573fda27ab0502c7c253e2b2. This device is marketed under the brand name UXII PACK-SED. The license holder is Sysmex 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
CELLPACK DFL
UID: IMP/IVD/2019/000255_8d6f74525be560685b3609a84e8770fd_afb81585573fda27ab0502c7c253e2b2

Brand Name

UXII PACK-SED

Device Class

Class B

Approving Authority

CDSCO

Product Information

Whole blood diluent for use in hematology analyzers

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