RAPID TEST FOR P. FALCIPARUM MALARIA
- UID
- MFG/IVD/2020/000118_dae11344f9bb752953f267afd6827066_12e5903b5f3dc831a7c0a4f3c27a7aa9
- Device class
- Class C
- Brand name
- PARACHECK PF DEVICE
- Approving authority
- Sub Zonal Goa
- Product information
- Paracheck Pf is a rapid self performing, qualitative, two site sandwich immunoassay for the determination of P. falciparum specific histidine rich protein –2 (PARACHECK PF DEVICE) in whole blood samples. Paracheck Pf detects the presence of Pf HRP-2 in whole blood specimen and is a sensitive and specific test for the detection of P. falciparum malaria
RAPID TEST FOR P. FALCIPARUM MALARIA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000118_dae11344f9bb752953f267afd6827066_12e5903b5f3dc831a7c0a4f3c27a7aa9. This device is marketed under the brand name PARACHECK PF DEVICE. The license holder is ORCHID BIOMEDICAL SYSTEMS A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is Sub Zonal Goa.
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.