Creatine kinase-MB
- UID
- MFG/IVD/2021/000017_a85501e62508d30eb524002feb1f982a_8269bc8e6cab8d662cff2795cdd2fdaf
- Device class
- Class B
- Brand name
- ISEPAK / TURBOLYTE ISEPAK / ISEPAK-ER
- License holder
- AGD BIOMEDICALS P LTD
- Approving authority
- Kokan Division
- Product information
- It is intended for in vitro quantitative determination of CK MB levels in Serum and Plasma
Creatine kinase-MB is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000017_a85501e62508d30eb524002feb1f982a_8269bc8e6cab8d662cff2795cdd2fdaf. This device is marketed under the brand name ISEPAK / TURBOLYTE ISEPAK / ISEPAK-ER. The license holder is AGD BIOMEDICALS P LTD, and it is classified as Device Class Class B. The approving authority is Kokan Division.
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.