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ISE Diluent - India CDSCO Medical Device Registration

ISE Diluent is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000241_fde6d5730f575f135e8f7c2c1d3b3a39_9a73ac9c65e5f53aba1a2478808e881a. This device is marketed under the brand name Elitech Clinical Systems SAS. The license holder is Q-Line Biotech Private Limited (Formerly Known As POCT SERVICES PRIVATE LIMITED), 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
ISE Diluent
UID: IMP/IVD/2022/000241_fde6d5730f575f135e8f7c2c1d3b3a39_9a73ac9c65e5f53aba1a2478808e881a

Brand Name

Elitech Clinical Systems SAS

Device Class

Class B

Approving Authority

CDSCO

Product Information

Elitech Clinical Systems ISE Diluent is used for quatitative determination of sodium(Elitech Clinical Systems SAS), potassium (Elitech Clinical Systems SAS), chloride (Elitech Clinical Systems SAS) and carbon dioxide (Elitech Clinical Systems SAS) in human serum and plama on ELITech Clinical instruments equipped with ISE module

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