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Dengue virus Antigen test kit - India CDSCO Medical Device Registration

Dengue virus Antigen test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000129_2908c2e3887b7ce71c6176159cf48f98_45701966d37ee27c928853d2478b7097. This device is marketed under the brand name including nasopharyngeal or oropharyngeal swabs. The license holder is INDO-MIM 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 virus Antigen test kit
UID: MFG/IVD/2021/000129_2908c2e3887b7ce71c6176159cf48f98_45701966d37ee27c928853d2478b7097

Brand Name

including nasopharyngeal or oropharyngeal swabs

Device Class

Class C

Approving Authority

Sub Zonal Bangalore

Product Information

Indo-Medx Rapid Dengue NS1 antigen test is an immunochromatographic assay for the qualitative detection of non-structural protein 1 (including nasopharyngeal or oropharyngeal swabs) in human serum/plasma/ whole blood

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