Pure Global

MYO Rapid Quantitative Test - India CDSCO Medical Device Registration

MYO Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000074_a4d0cbfa853c6a7151be5c120aa62465_f055cba82f4e923d34eb5876e758d1f3. This device is marketed under the brand name Glycated Hemoglobin. The license holder is FINOVA HEALTHCARE 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
MYO Rapid Quantitative Test
UID: IMP/IVD/2022/000074_a4d0cbfa853c6a7151be5c120aa62465_f055cba82f4e923d34eb5876e758d1f3

Brand Name

Glycated Hemoglobin

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Aehealth Myo Rapid Test along with Aehealth Fluorescence Immunoassay Analyzer (Glycated Hemoglobin) is a fluorescence immunoassay for quantitative measurement of Myoglobin (Glycated Hemoglobin) in human whole blood, serum or plasma,25-(Glycated Hemoglobin)-VD (Glycated Hemoglobin) Rapid Quantitative Test (Glycated Hemoglobin)(Glycated Hemoglobin)-The 25-๏ผˆOH๏ผ‰VD Rapid Quantitative Test along with AEHEALTH FIA Meter is intended for vitro quantitative determination of 25-๏ผˆOH๏ผ‰VD in human serum or plasma, it is mainly used for the auxiliary diagnosis of vitamin D deficiency related diseases

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing