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RAPID TEST FOR P. FALCIPARUM MALARIA - India CDSCO Medical Device Registration

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_8774112d39ccb6f29963d4e600a7d3c1. 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.

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CDSCO Registered
Class Class C
RAPID TEST FOR P. FALCIPARUM MALARIA
UID: MFG/IVD/2020/000118_dae11344f9bb752953f267afd6827066_8774112d39ccb6f29963d4e600a7d3c1

Brand Name

PARACHECK PF DEVICE

Device Class

Class C

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 โ€“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.

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