Abbott Proteinase K Recombinant, PCR Grade

Alinity m HIV-1 Application Specification File

Alinity m HCV Application Specification File

Alinity m STI Application Specification File

Abbott RealTime CMV m2000 System Combined Application CD-ROM

Abbott RealTime CMV Calibrator Kit

Abbott RealTime CMV Control Kit

Abbott RealTime CMV Amplification Reagent Kit

Alinity m EBV Application Specification File

Alinity m CMV Application Specification File

Alinity m CMV Application Specification File

Alinity m CMV CAL Kit

Alinity m CMV CTRL Kit

Alinity m CMV AMP Kit

Alinity m HSV 1 & 2 / VZV Application Specification File

Alinity m HSV 1 & 2 / VZV CTRL Kit

Alinity m HSV 1 & 2 / VZV AMP Kit

Knowledge Base Update for VITEK2 Software

R3.1 SW/FW for BACT/ALERT VIRTUO

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli

VITEK® 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli

VITEK® MS knowledge base v3.3

ETEST® is a manual, quantitative technique for determination of antimicrobial susceptibility of non-fastidious Gram-negative and Gram-positive aerobic bacteria and fastidious bacteria

ETEST® is a manual, quantitative technique for determination of antimicrobial susceptibility of non-fastidious Gram-negative and Gram-positive aerobic bacteria and fastidious bacteria

ETEST® is a manual, quantitative technique for determination of antimicrobial susceptibility of non-fastidious Gram-negative and Gram-positive aerobic bacteria and fastidious bacteria

ETEST® is a manual, quantitative technique for determination of antimicrobial susceptibility of non-fastidious Gram-negative and Gram-positive aerobic bacteria and fastidious bacteria

VITEK MS ready to use reagent for calibration and fine tuning of the VITEK MS instrument

AccuDiag ™ Varicella-Zoster Virus (VZV) IgG Enzyme-linked Immunosorbent Assay (ELISA) is intended for the detection and quantitative determination of IgG antibody to VZV in human sera.

AccuDiag ™Mycoplasma pneumoniae IgM Test System provides a means for the qualitative detection of IgM antibodies to Mycoplasma pneumoniae in human sera.

AccuDiag™ Taenia.solium (Cysticercosis) IgG ELISA -For the qualitative and/or quantitative detection of immunoglobulin G (IgG) antibodies to Taenia solium in a clinical specimen, using an enzyme immunoassay (EIA) method.

AccuDiag™ Fasciola IgG ELISA

AccuDiag™ Echinococcus IgG ELISA

AccuDiag™ Trichinella IgG ELISA - For the qualitative detection of immunoglobulin G (IgG) antibodies to the parasitic nematode Trichinella species in a clinical specimen, using an enzyme immunoassay (EIA) method.

AccuDiag™ Schistosoma IgG ELISA - For the qualitative detection of immunoglobulin G (IgG) antibodies to multiple species of the parasitic flatworm Schistosoma in a clinical specimen, using an enzyme immunoassay (EIA) method.

AccuDiag™ Ascaris IgG ELISAFor the qualitative detection of immunoglobulin G (IgG) antibodies to the parasitic nematode Ascaris lumbricoides in a clinical specimen, using an enzyme immunoassay (EIA) method.

In Vitro Diagnostic Test kit for the determination of Procalcitonin in human whole blood, plasma or serum

In Vitro Diagnostic Test kit for the determination of Procalcitonin in human whole blood, serum and plasma

The Nano-Check™ Influenza+COVID-19 Dual Test is a lateral flow immunochromatographic assay intended for in vitro rapid, simultaneous qualitative detection and differentiation of influenza A, and influenza B nucleoprotein antigens and SARS-CoV-2 nucleocapsid antigen directly from anterior nasal swab specimens of individuals with signs and symptoms of respiratory infection consistent with COVID-19 within the first five (5) days of symptom onset when tested at least twice over three days with at least 48 hours between tests. Clinical signs and symptoms of respiratory viral infection due to SARS-CoV-2 and influenza can be similar. The Nano-Check™ Influenza+COVID-19 Dual Test is only for in vitro diagnostic use under the Food and Drug Administration’s Emergency Use Authorization. This product has not been cleared or approved.

The Nano-Check RSV Test is a rapid immunochromatographic assay for the qualitative detection of respiratory syncytial virus (RSV) nucleoprotein antigen in anterior nasal swab specimens from patients with signs and symptoms of respiratory infection. This test is intended for in vitro diagnostic use to aid in the diagnosis of RSV infections in infants and pediatric patients aged 6 months to 6 years old, and adults over 60 years of age.

Fluorescence In Vitro diagnostic test kit for the detection of Procalcitonin in human whole blood, serum or plasma

JOURNEY II AP CUTTING BLOCK - SIZE 3