Diagnostic Kit for Beta-HCG
- UID
- IMP/IVD/2023/000208_965b4e737ac0bb5ed5019976c63f603b_ee841544c999a1bc7a0921c0fec72d7f
- Device class
- Class C
- Brand name
- MyBox SAA
- License holder
- Mylab Discovery Solutions Pvt. Ltd.
- 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
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.