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HbSAg RAPID TEST KIT - India CDSCO Medical Device Registration

HbSAg RAPID TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000082_58a59e04c071e1f24ae76612eae8eef4_0dea597c3268cdc70b555ff6798a8606. The license holder is PEERLESS BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is Central Drug Standard Control Organisation, South 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 TEST KIT
UID: MFG/IVD/2022/000082_58a59e04c071e1f24ae76612eae8eef4_0dea597c3268cdc70b555ff6798a8606

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

The HBsAg Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of hepatitis B surface antigen ##PLACEHOLDER_0## in human serum or plasma or Whole Blood

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