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HBsAg Rapid Diagnostic Test Kit - India CDSCO Medical Device Registration

HBsAg Rapid Diagnostic Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000164_0e5b7301d584aadc2401b53db722bfd8_6fe807cfda64e671d8e0fe27c5c84b07. This device is marketed under the brand name AccuTest HBsAg Rapid Diagnostic Test Kit. The license holder is Accurex Biomedical Pvt Ltd, 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
HBsAg Rapid Diagnostic Test Kit
UID: MFG/IVD/2022/000164_0e5b7301d584aadc2401b53db722bfd8_6fe807cfda64e671d8e0fe27c5c84b07

Brand Name

AccuTest HBsAg Rapid Diagnostic Test Kit

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

AccuTest HBsAg intended to be used for qualitative detection of Hepatitis B surface antigen (AccuTest HBsAg Rapid Diagnostic Test Kit) in serum/plasma/whole blood

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