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HBV antigen detection ELISA kit - India CDSCO Medical Device Registration

HBV antigen detection ELISA kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000109_3457919814dbb8a5cab237d42ef82b4d_75e75a1049b951c89d7f1bfdde812b24. The license holder is Levram Lifesciences Private Limited, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class D
HBV antigen detection ELISA kit
UID: MFG/IVD/2022/000109_3457919814dbb8a5cab237d42ef82b4d_75e75a1049b951c89d7f1bfdde812b24

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

This kit is qualitative detection of HBsAg in human serum or plasma. It is intended for diagnosing of patients related to infection with hepatitis B virus

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