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GLYCOSYLATEDHEMOGLOBIN REAGENT KIT - India CDSCO Medical Device Registration

GLYCOSYLATEDHEMOGLOBIN REAGENT KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000080_f205d3bb5448b8870d496e6e55309cbb_e6eab045c2d9b4f96d4fd3f84d496e2f. This device is marketed under the brand name LDH. The license holder is Dhiti Diagnostics Private Limited, and it is classified as Device Class Class B. The approving authority is Uttarakhand.

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
GLYCOSYLATEDHEMOGLOBIN REAGENT KIT
UID: MFG/IVD/2021/000080_f205d3bb5448b8870d496e6e55309cbb_e6eab045c2d9b4f96d4fd3f84d496e2f

Brand Name

LDH

Device Class

Class B

Approving Authority

Uttarakhand

Product Information

In vitro quantitative determination of glycosylated Hemoglobin HbA1c in human whole blood

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