CDSCO UID MFG/IVD/2022/000109_52260464ef102e34065d11c96ad554f9_73a267147fb21fd7e5f39481a80fe67d

Syphilis Antibody Rapid Test kit

Levram Lifesciences Private Limited·Device Class Class D·India CDSCO
Registration details
UID
MFG/IVD/2022/000109_52260464ef102e34065d11c96ad554f9_73a267147fb21fd7e5f39481a80fe67d
Device class
Class D
Approving authority
Central Drug Standards Control Organization, West Zone
Product information
The Syphilis antibody rapid test kit ##PLACEHOLDER_0## is a rapid chromatographic immunoassay for the qualitative detection of antibodies ##PLACEHOLDER_0## to Treponema Pallidum ##PLACEHOLDER_0## in the whole blood, Serum or Plasma to aid in the diagnosis of syphilis
Other products from Levram Lifesciences Private Limited
Products from the same license holder (10 products)
Malaria Pf/Pv Rapid Diagnostic test kit
Class C
RNA Extraction kit
Class C
HIV 1/2 and Syphilis Ab Detection dual test kit
Class D
HCV antibody detection ELISA kits
Class D
HIV detection ELISA kit
Class D
Dengue combo kit
Class C
Dengue NS1 ELISA kit
Class C
Dengue NS1 Rapid Antigen Test
Brand: Pf. HRP-2
Class C
HIV 1/2 Antibody Detection Rapid Test kit
Class D
Malaria Pf /Pan antigen rapid test kit
Class C
About this record

Syphilis Antibody Rapid Test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000109_52260464ef102e34065d11c96ad554f9_73a267147fb21fd7e5f39481a80fe67d. The license holder is Levram Lifesciences Private Limited, and it is classified as Device Class Class D. 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.