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Gamma GT Diagnostic Kit - India CDSCO Medical Device Registration

Gamma GT Diagnostic Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000144_9071a77b54cafa5e8d2312e08dc24b69_9e2d35e9ea7787ecdde5eb521592ccfb. 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
Gamma GT Diagnostic Kit
UID: MFG/IVD/2022/000144_9071a77b54cafa5e8d2312e08dc24b69_9e2d35e9ea7787ecdde5eb521592ccfb

Brand Name

LDH โ€“ DGKC

Device Class

Class B

Approving Authority

Karnataka

Product Information

The ๏‹-GT test system is a device intended for the quantitative in vitro determination of L-ห -Glutamyltransferase (LDH โ€“ DGKC) activity in serum and plasma. This product is suitable for manual use and on semi-automated systems

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