Specimen Collection Container

Digital Dry Bath

Digital Dry Bath

BioFire® Global Fever Special Pathogens Panel - IVD reagent kit containing 6 tests

BIOFIRE® SHIELD™ Control Kit for the BioFire Global Fever Special Pathogens Panel - IVD Reagent External Control Kit

The VITEK REVEAL Instrument is a benchtop instrument that processes up to four AST tests . Installation and operating details for the Reveal Instrument are provided in this manual.

The VITEK REVEAL SEALER provides the heat welding of the VITEK REVEAL SENSOR PANEL to the 96 well AST Drug Plate.

The VITEK REVEAL Reveal AST Assays are indicated for susceptibility testing of pathogenic bacteria

QMedix™Toxoplasma Gondii IgG ELISA KitThis test is intended for the qualitative and/or quantitative detection of immunoglobulin G (IgG) antibodies to the parasitic protozoan Toxoplasma gondii in a clinical specimen, using an enzyme immunoassay (EIA) method.

QMedix™ Rubella IgG ELISAThis test is intended to be used for the qualitative and/or quantitative detection of immunoglobulin G (IgG) antibodies to Rubella virus in a clinical specimen, using an enzyme immunoassay (EIA) method.

AccuDiag ™ Rubella IgM Enzyme- Linked Immunosorbent Assay (ELISA) is intended for the in vitro qualitative determination of IgM antibodies in human serum and as an aid in the diagnosis of current or recent infection with Rubella virus

AccuDiag ™ Herpes Simplex 1 IgG (HSV 1 IgG) ELISA

AccuDiag ™Herpes Simplex 2 IgG (HSV 2 IgG) ELISA

QMedix™ Lyme IgG/IgM ELISAThis test is intended to be used for the qualitative and/or quantitative detection of immunoglobulin G (IgG) and immunoglobulin M (IgM) antibodies to Borrelia burgdorferi in a clinical specimen, using an enzyme immunoassay (EIA) method.

QMedix™ Herpes Simplex 1,2 IgM (HSV 1,2 IgM) ELISA is an enzyme-linked immunosorbent assay for the qualitative detection of IgM class antibodies to Herpes Simplex Virus (HSV) in human serum. This test is intended to be used to evaluate serologic evidence of primary or reactivated infection with HSV and is for In Vitro diagnostic use.

QMedix™ EBV VCA IgG ImmunoFlourescent Assay

Sperm Morphology Quality Control - Stained 2 Pap stained and coverslipped glass sperm morphology smears, 2 levels - a high and a low value. https://www.fertilitysolutions.com/product-category/sperm-morphology-quality-control

Sperm Viability Quality Control. 2 stained and coverslipped sperm viability smears, 2 levels - a high and a low value.https://www.fertilitysolutions.com/product-category/sperm-viability-quality-control

Sperm Morphology Quality Control - Unstained. 2 unstained, fixed, glass sperm morphology smears, 2 levels - a high and a low value. https://www.fertilitysolutions.com/product-category/sperm-morphology-quality-control

Sperm Morphology Virtumorph® Quality Control - 1 fifty cell Virtumorph® printed virtual semen morphology smear and 1 Pap stained and coverslipped glass sperm morphology smear, 2 levels - a high and a low value.https://www.fertilitysolutions.com/product-category/sperm-morphology-quality-control

Purple Vitrification Device (Pack of 10) cryo-GO Vitrification Device is a cryopreservation device intended for use in vitrification procedures to contain and maintain human oocytes (MII), pronuclear (PN) zygotes through day 3 cleavage stage embryos and blastocysts stage embryos.

100 test kit

220 test kits

Sepsis Host Response US IVD EDTA PAXgene Variant Cartridge

ClearFit 1.4cm Cover with Slot

ClearFit & InvisiShunt Conveniece Kit

FebriDx® Bacterial / Non-Bacterial Point of Care Assay Test Kit, 25 tests

ViraDx™ SARS-CoV-2/Flu A+B Rapid Antigen Test Kit, 25 tests

Reference material to monitor the performance of the in vitro quantitative detection of BCR-ABL1 and ABL1 mRNA transcripts for Xpert BCR-ABL Ultra assay on the Cepheid GeneXpert system.

POS external qc to monitor the performance of in vitro laboratory nucleic acid testing procedures for the qualitative detection of pathogens included in BIOFIRE SPOTFIRE R Panel and SPOTFIRE R Panel Mini

NEG external qc to monitor the performance of in vitro laboratory nucleic acid testing procedures for the qualitative detection of pathogens included in the BIOFIRE SPOTFIRE R Panel and SPOTFIRE R Panel Mini

The Know Rapid STD Screening Kit (Urine Test Cassette) includes individual test cassettes for:1. Chlamydia Trachomatis (CHT)2. Neisseria Gonorrhoeae (NGH)3. Trichomonas Vaginalis (TV)4. Mycoplasma Genitalium (MG).Each test strip in the cassette is suitable for urine specimen tests. During testing, if a specific antigen presented in the urine specimen reacts with each test cassette in the Treagent area, the conjugate antigens complex will be bound with the test cassette’s antibody coated on the membrane in case of a positive result. This would show in a darkred colored line in the T line region of a positive result. In case of negative result, no conjugate would bind at the test cassette’s antibody in the T line region and no line would form in the T line region of the test membrane. The C line serves as an internal qualitative control of the test system to indicate that an adequate volume of specimen has been applied and the flow occurred. Absence of C line indicates an invalid test result.

The MobiLab Standard Sexual Health Self Screening Kit (urine specimen) includes individual test cassettes for:1. Trichomonas Vaginalis (TV)2. Candida Albicans (Yeast) (CA)3. Gardnerella Vaginalis (GV)4. Mycoplasma Genitalium (MG)5. Chlamydia Trachomatis (CHT)6. Neisseria Gonorrhoeae (NGH).Each test strip in the cassette is suitable for urine specimen tests. During testing, if a specific antigen presented in the urine specimen reacts with each test cassette in the Treagent area, the conjugate antigens complex will be bound with the test cassette’s antibody coated on the membrane in case of a positive result. This would show in a darkred colored line in the T line region of a positive result. In case of negative result, no conjugate would bind at the test cassette’s antibody in the T line region and no line would form in the T line region of the test membrane. The C line serves as an internal qualitative control of the test system to indicate that an adequate volume of specimen has been applied and the flow occurred. Absence of C line indicates an invalid test result.

Culture Media, Selective and Non-Differential

Culture Media, Selective and Non-Differential

Culture Media, Selective and Non-Differential

Culture Media, Selective and Non-Differential

Culture Media, Selective and Non-Differential

Culture Media, Selective and Non-Differential

Culture Media, Enriched

Culture Media, Selective and Non-Differential

Culture Media, Selective and Non-Differential

Cultured Media, Non-Selective and Non-Differential

Culture Media, Selective and Non-Differential

Culture Media, Selective and Non-Differential