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Diagnostics test reagent / kits for Neutrophil Gelatinase-related Lipid Carrier Protein Test Kit - India CDSCO Medical Device Registration

Diagnostics test reagent / kits for Neutrophil Gelatinase-related Lipid Carrier Protein Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000163_f264c64b93f201e1d526e1c78ed26206_c802df8a03ad11120c9e73b85581f94d. This device is marketed under the brand name hCG. The license holder is M/s Allied Biotechnology India Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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CDSCO Registered
Class Class B
Diagnostics test reagent / kits for Neutrophil Gelatinase-related Lipid Carrier Protein Test Kit
UID: MFG/IVD/2020/000163_f264c64b93f201e1d526e1c78ed26206_c802df8a03ad11120c9e73b85581f94d

Brand Name

hCG

Device Class

Class B

Approving Authority

Kokan Division

Product Information

It is used for in vitro quantitative detection of Neutrophil Gelatinase-related Lipid Carrier Protein (hCG) (hCG) content in human serum, plasma or whole blood

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