Pure Global

SFRI Diluent 5.1 - India CDSCO Medical Device Registration

SFRI Diluent 5.1 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000663_c9a46ed9658944d7ab545fb075490b38_3f5c4917a30d3347a93b5a4e1facc7aa. The license holder is Genworks Health 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
SFRI Diluent 5.1
UID: IMP/IVD/2020/000663_c9a46ed9658944d7ab545fb075490b38_3f5c4917a30d3347a93b5a4e1facc7aa

Device Class

Class B

Approving Authority

CDSCO

Product Information

SFRI Diluent 5.1 is used by SFRIโ€™s 5 part diff blood cell counters as a diluing reagent

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name or brand