Diagnostic Kit for TSH - India CDSCO Medical Device Registration

Diagnostic Kit for TSH is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000208_c420a800c79d99f6ab7f05b1989a6c25_0b63d5ebe2f4b4fc5f1efabd7db5de31. 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

CDSCO Registered

Class Class B

Diagnostic Kit for TSH

UID: IMP/IVD/2023/000208_c420a800c79d99f6ab7f05b1989a6c25_0b63d5ebe2f4b4fc5f1efabd7db5de31

Brand Name

MyBox HbA1c

License Holder

Mylab Discovery Solutions Pvt. Ltd.

Device Class

Class B

Approving Authority

CDSCO

Product Information

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