Diagnostic Kit for Beta-HCG - India CDSCO Medical Device Registration

Diagnostic Kit for Beta-HCG is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000208_965b4e737ac0bb5ed5019976c63f603b_ee841544c999a1bc7a0921c0fec72d7f. This device is marketed under the brand name MyBox SAA. The license holder is Mylab Discovery Solutions Pvt. Ltd., and it is classified as Device Class Class C. 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 C

Diagnostic Kit for Beta-HCG

UID: IMP/IVD/2023/000208_965b4e737ac0bb5ed5019976c63f603b_ee841544c999a1bc7a0921c0fec72d7f

Brand Name

MyBox SAA

License Holder

Mylab Discovery Solutions Pvt. Ltd.

Device Class

Class C

Approving Authority

CDSCO

Product Information

This kit is suitable for in vitro quantitative detection of the concentration of Human Chorionic Gonadotropin beta-Subunit (MyBox SAA) in human serum, plasma and whole blood