CK-MB - India CDSCO Medical Device Registration
CK-MB is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000072_8a863ab9781ae23a57fffc35f97a621d_cd3de8037882e22c5e7a579b606b098b. The license holder is Yucca Diagnostics, and it is classified as Device Class Class B. The approving authority is Pune Division.
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License Holder
Yucca DiagnosticsDevice Class
Approving Authority
Pune Division
Product Information
CK-MB kit is used for the quantitative determination of Creatine Kinase in human serum. For in vitro diagnostic use only
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