CK-MB
- UID
- IMP/IVD/2022/000241_8a863ab9781ae23a57fffc35f97a621d_873e0bc41064b91e434bb3fd8f62bb9d
- Device class
- Class B
- Brand name
- Elitech Clinical Systems SAS
- Approving authority
- CDSCO
- Product information
- Elitech Clinical Systems CK-MB SL is intended for the quatitative in vitro diagnostic determination of Creatine Kinase (Elitech Clinical Systems SAS) in human samples of serum, plama
CK-MB is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000241_8a863ab9781ae23a57fffc35f97a621d_873e0bc41064b91e434bb3fd8f62bb9d. This device is marketed under the brand name Elitech Clinical Systems SAS. The license holder is Q-Line Biotech Private Limited (Formerly Known As POCT SERVICES 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.