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Influenza A/B Antigen Test Kit - India CDSCO Medical Device Registration

Influenza A/B Antigen Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000068_d29c26089f69538afcab6c9ee7321798_7024f8368197878b236afd8d3d1c2287. This device is marketed under the brand name PathKits Simple COVID-19 Ag Rapid Kit. The license holder is PATHKITS HEALTHCARE PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is Sub Zonal Baddi.

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
Influenza A/B Antigen Test Kit
UID: MFG/IVD/2021/000068_d29c26089f69538afcab6c9ee7321798_7024f8368197878b236afd8d3d1c2287

Brand Name

PathKits Simple COVID-19 Ag Rapid Kit

Device Class

Class C

Approving Authority

Sub Zonal Baddi

Product Information

Influenza A/B Antigen Test is a rapid chromatographic immunoassay for the qualitative detection of Influenza A and B antigens in nasal swab or Nasopharyngeal Swab or Saliva or Oral Swab specimens. It is intended to aid in the rapid differential diagnosis of influenza A and B viral infections

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