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CREATININE DIAGNOSTIC KIT - India CDSCO Medical Device Registration

CREATININE DIAGNOSTIC KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000144_97d27305c5abf257a70c8c5cbd718a36_acbf8ba5aab816568633d0571de3e3b0. This device is marketed under the brand name LDH โ€“ DGKC. The license holder is Randox Laboratories (India) Pvt.Ltd, and it is classified as Device Class Class B. The approving authority is Karnataka.

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CDSCO Registered
Class Class B
CREATININE DIAGNOSTIC KIT
UID: MFG/IVD/2022/000144_97d27305c5abf257a70c8c5cbd718a36_acbf8ba5aab816568633d0571de3e3b0

Brand Name

LDH โ€“ DGKC

Device Class

Class B

Approving Authority

Karnataka

Product Information

The Creatinine (LDH โ€“ DGKC) device is intended for the quantitative in vitro determination of creatinine in serum, plasma or urine. This product is suitable for manual use and on semi-automated analyzers

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