INTENDED USE The Malaria Gold Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of antibodies including IgG, IgM and IgA to Plasmodium falciparum (Pf) and vivax, ovale, and malariea (Pv.o.m) in whole blood. This device is intended to be used as a screening test and as an aid in the diagnosis of infection with Plasmodium. Any reactive specimen with the Malaria Gold Rapid Test must be confirmed with alternative testing method(s) and clinical findings. REAGENTS AND MATERIALS PROVIDED 1. Each kit contains 25 test devices, each sealed in a foil pouch with three items inside: a. One cassette device. b. One plastic dropper. c. One desiccant. 2. Sample diluent (1 vial, 5 ml) 3. One package insert (instruction for use). MATERIALS REQUIRED BUT NOT PROVIDED 1. Clock or Timer 2. Lancing device for whole blood test
The Pathocatch Coviself Covid - 19 Rapid Antigen test (RAT) is an in vitro diagnostic test for the qualitative detection of covid - 19 antigen in nasal swab specimens directly from individuals with or without symptoms or other epidemiological reasons to suspect COVID-19.
RT PCR-Detection Kit
Viral Transport Kit
Uncut Sheet Influenza A/B Rapid Test Specimen:nasal swab Intended Use The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens. Principle The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. Storage and Stability 1.Store as packaged in the sealed pouch at room temperature or refrigerated (4-30 or 40-86). The test device is stable through the expiration date printed on the sealed pouch. 2.The test must remain in the sealed pouch until use.
FFP2 Vertical-Flat Valved Respirator Face Mask CE certified by CCQS Ireland (NB no. 2834) Tested and certified according to EN 149:2001+A1:2009 Module Type of Certification: Module B + Module C2 Class: FFP2 This respirator mask is certified and classified as FFP2 under EU standard EN 149:2001+A1:2009. EN 149:2001+A1:2009 - Respiratory protective devices - Filtering half masks to protect against particles. This European Standard specifies the minimum requirements for filtering half masks used as respiratory protective devices, specifically against particles, and the required laboratory and practical performance tests to assess masks' compliance. EN 149:2001+A1:2009 classified half masks into three types according to their filtering capacities: FFP1, FFP2 and FFP3. Respirators that meet the requirements of EN 149:2001+A1:2009 are designed to protect against solids, water-based aerosols, and oil-based aerosols. FFP2 masks have a minimum of 94% filtration percentage and maximum 8% leakage to the inside. They are mainly used in construction, agriculture, and by healthcare professionals against influenza viruses.
Rapid antigen test kits , viral transport media ( moh approved vtm kits), rna extraction kits , cr plates and machines. biochemistry analyser , biochemistry medias fda approved rapid test kits hiv , hcv , filter tips, laboratory consumables , agar plates , wolf air mask (the only device globally to be tested and effective 99.9 percent against covid 19).Export
Isolation Gown
Gloves
Head Cover
Surgical Kit
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MSN Needle
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Flashback Needle
Patient ID
Micro Pipette Fixed & Variables
Latex Tourniquet