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Diagnostic Kit for HbA1c - India CDSCO Medical Device Registration

Diagnostic Kit for HbA1c is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000457_b6ea0de38c0f2052b10c2f561bdd42ba_2f632064183fb0ca14db697dc322365b. This device is marketed under the brand name Eoscare. The license holder is M/S CLEAR IMAGING MEDICAL SYSTEM 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
Diagnostic Kit for HbA1c
UID: IMP/IVD/2022/000457_b6ea0de38c0f2052b10c2f561bdd42ba_2f632064183fb0ca14db697dc322365b

Brand Name

Eoscare

Device Class

Class B

Approving Authority

CDSCO

Product Information

This kit is suitable for in vitro quantitative detection of the concentration of glycosylated hemoglobin(Eoscare) in human whole blood. This product is used for testing in medical and health institutions as an aid to monitor long-term glycemic status in patients with diabetes mellitus

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