CDSCO UID MFG/IVD/2020/000004_754d6bb7b58d01c017428c83bf519f11_a4e159da251274b73e7598576a4a74ac

KARWA COVID-19 RT-LAMP DIAGNOSTIC KIT

KARWA ENTERPRISES PRIVATE LIMITED·Device Class Class C·India CDSCO
Registration details
UID
MFG/IVD/2020/000004_754d6bb7b58d01c017428c83bf519f11_a4e159da251274b73e7598576a4a74ac
Device class
Class C
Approving authority
CDSCO -North Zone, Ghaziabad
Product information
Intended for qualitative detection of nucleic acid from SARS-CoV-2 RNA in throat and or nasal swab samples who are suspected of COVID-19
Other products from KARWA ENTERPRISES PRIVATE LIMITED
Products from the same license holder (10 products)
Malaria Pf Antigen Rapid Test
Class C
Syphilis Rapid Strip Test
Class D
Drugs of Abuse Rapid Test
Class C
Dengue NS1 ELISA Test Kit
Class C
HCV Rapid Card Test Kit
Class D
Syphilis Rapid Card Test
Class D
Typhoid Antigen Rapid Card Test
Class C
Syphilis ELISA Kit
Class D
HIV ELISA Test Kit
Brand: 3rd Generation
Class D
HIV ELISA Test Kit
Brand: 3rd Generation
Class D
About this record

KARWA COVID-19 RT-LAMP DIAGNOSTIC KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000004_754d6bb7b58d01c017428c83bf519f11_a4e159da251274b73e7598576a4a74ac. The license holder is KARWA ENTERPRISES PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

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.