Dengue NS1 Rapid Antigen Test
- UID
- MFG/IVD/2022/000109_7b2548ce54951d0031cf42487d2ca6f7_ba7a9105afeaac01ffd2f4a7d80f78d4
- Device class
- Class C
- Brand name
- Pf. HRP-2
- License holder
- Levram Lifesciences Private Limited
- Approving authority
- Central Drug Standards Control Organization, West Zone
- Product information
- Dengue NS1 Rapid Antigen Test is a medical device intended for the detection of Dengue virus Antigen in blood/body fluids.
Dengue NS1 Rapid Antigen Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000109_7b2548ce54951d0031cf42487d2ca6f7_ba7a9105afeaac01ffd2f4a7d80f78d4. This device is marketed under the brand name Pf. HRP-2. The license holder is Levram Lifesciences Private Limited, and it is classified as Device Class Class C. 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.