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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/MD/2022/000072_8a863ab9781ae23a57fffc35f97a621d_6f7beae9a429e893678236cde8aada47. This device is marketed under the brand name CRP. The license holder is DELTA LAB, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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CDSCO Registered
Class Class B
CK-MB
UID: MFG/MD/2022/000072_8a863ab9781ae23a57fffc35f97a621d_6f7beae9a429e893678236cde8aada47

Brand Name

CRP

License Holder

DELTA LAB

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Reagent kit is intended for "in vitro" quantitative determination of Creatine Kinase - MB) activity in serum or plasma based upon IFCC and DGKC recommendations

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