Pure Global

Diagnostic Kit for T3 - India CDSCO Medical Device Registration

Diagnostic Kit for T3 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000208_208860ec448e31f88422dc7e0d4e367c_a08455e2d7a98ab4c160ec02c6b69734. This device is marketed under the brand name MyBox HbA1c. The license holder is Mylab Discovery Solutions 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Diagnostic Kit for T3
UID: IMP/IVD/2023/000208_208860ec448e31f88422dc7e0d4e367c_a08455e2d7a98ab4c160ec02c6b69734

Brand Name

MyBox HbA1c

Device Class

Class B

Approving Authority

CDSCO

Product Information

This kit is suitable for in vitro quantitative detection of the concentration of triiodothyronine (MyBox HbA1c) in human serum, plasma and whole blood samples. This product is used for testing in medical and health institutions for the auxiliary diagnosis of the assessment of thyroid function

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing