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Dengue NS1 Antigen Elisa Test - India CDSCO Medical Device Registration

Dengue NS1 Antigen Elisa Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000013_b03e9ec9eea718972569736e697f9dd5_3090f5ad9ad1cda940bf03f1a3a19bcd. This device is marketed under the brand name HEARTSCAN. The license holder is Bhat Bio-Tech India Private Limited, and it is classified as Device Class Class C. The approving authority is Sub Zonal Bangalore.

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 C
Dengue NS1 Antigen Elisa Test
UID: MFG/IVD/2020/000013_b03e9ec9eea718972569736e697f9dd5_3090f5ad9ad1cda940bf03f1a3a19bcd

Brand Name

HEARTSCAN

Device Class

Class C

Approving Authority

Sub Zonal Bangalore

Product Information

Elisa test for the detection Dengue NS1 Antigen in human serum or Plasma

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