Total Beta Human Chorionic Gonadotropin eCLIA - India CDSCO Medical Device Registration

Total Beta Human Chorionic Gonadotropin eCLIA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000540_a059caeedc4b3103e6b385463559ec6b_7c9585aeaee63f58c5f5cfdd42954693. This device is marketed under the brand name Electrochemiluminescence immunoassay. The license holder is PSR Diagnostic Pvt Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

Total Beta Human Chorionic Gonadotropin eCLIA

UID: IMP/IVD/2021/000540_a059caeedc4b3103e6b385463559ec6b_7c9585aeaee63f58c5f5cfdd42954693

Brand Name

Electrochemiluminescence immunoassay

License Holder

PSR Diagnostic Pvt Ltd

Device Class

Class B

Approving Authority

CDSCO

Product Information

Immunoassay for in vitro quantitative determination of human chorionic gonadotropin in human serum and plasma. This assay is intended for use specially in assisting diagnosis and monitoring of pregnancy

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Total Beta Human Chorionic Gonadotropin eCLIA

Brand: eCLIA

Q-Line Biotech Private Limited (Formerly Known As POCT SERVICES PRIVATE LIMITED)

Class C

Automated ECL Immunoassay Analyzer

Brand: Electrochemiluminescence immunoassay

PSR Diagnostic Pvt Ltd

Total Beta Human Chorionic Gonadotropin eCLIA - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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Total Beta Human Chorionic Gonadotropin eCLIA

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