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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/2019/000287_c9a46ed9658944d7ab545fb075490b38_1f1f37464cf9ccb37312f09a094a758c. This device is marketed under the brand name Na+, K+,Cl-,Ca++, pH. The license holder is Edif Medical Systems, 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
SFRI Diluent 5.1
UID: IMP/IVD/2019/000287_c9a46ed9658944d7ab545fb075490b38_1f1f37464cf9ccb37312f09a094a758c

Brand Name

Na+, K+,Cl-,Ca++, pH

License Holder

Edif Medical Systems

Device Class

Class B

Approving Authority

CDSCO

Product Information

Diluent is a medical device used for blood diluting for further testing such as CBC

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