G6PD Detection Test - India CDSCO Medical Device Registration

G6PD Detection Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000021_b0ba556a474d992f52c8de1e67a8b488_3f1f509788324b5c609ad378b00c41e2. This device is marketed under the brand name Multigene-Multiplex Single tube format. The license holder is Mylab Discovery S0lutions Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.

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CDSCO Registered

Class Class C

G6PD Detection Test

UID: MFG/IVD/2020/000021_b0ba556a474d992f52c8de1e67a8b488_3f1f509788324b5c609ad378b00c41e2

Brand Name

Multigene-Multiplex Single tube format

License Holder

Mylab Discovery S0lutions Pvt. Ltd

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

The G6PD detection test is a quantitative biochemical test for determination of Glucose 6 Phosphate dehydrogenase concentration(Multigene-Multiplex Single tube format) in Dried blood spots (Multigene-Multiplex Single tube format) intended for screening of Glucose 6 Phosphate dehydrogenase deficiency in newborn

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Brand: Multigene-Multiplex Single tube format

Mylab Discovery S0lutions Pvt. Ltd

G6PD Detection Test - India CDSCO Medical Device Registration

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Device Class

Approving Authority

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