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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 MFG/IVD/2020/000109_31b87420c6b6522fe3083f01061c1d47_58dbce5995859072cbdabd36dab35fef. This device is marketed under the brand name 3 part Differential. The license holder is Promea Therapeutics Private Limited, and it is classified as Device Class Class B. The approving authority is Telangana.

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: MFG/IVD/2020/000109_31b87420c6b6522fe3083f01061c1d47_58dbce5995859072cbdabd36dab35fef

Brand Name

3 part Differential

Device Class

Class B

Approving Authority

Telangana

Product Information

For Dilution of whole blood sample for Hematological Analysis by Hematology Analyser

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