Saline Solution is a diluent used for manual preparation of organism suspensions
Saline Solution is a diluent used for manual preparation of organism suspensions, prior to identification and antimicrobial susceptibility processing with VITEK® 2 instruments.
LON,LTW
SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION,Suscepti
SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION,Susceptibility test cards, antimicrobial
Saline Solution is a diluent used for manual preparation of organism suspensions
Saline Solution is a diluent used for manual preparation of organism suspensions, prior to identification and antimicrobial susceptibility processing with VITEK® 2 instruments.
LTW,LON
Susceptibility test cards, antimicrobial,SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL
Susceptibility test cards, antimicrobial,SYSTEM, TEST, AUTOMATED, ANTIMICROBIAL SUSCEPTIBILITY, SHORT INCUBATION
This single-use tips are used by the VIDAS®3 pipetting unit to pipette the sampl
This single-use tips are used by the VIDAS®3 pipetting unit to pipette the samples according to the defined loading plan.
LXG
EQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE
Isolation, enumeration and direct or presumptive identification of urinary tract
Isolation, enumeration and direct or presumptive identification of urinary tract infection organisms
Chromogenic medium for the selective isolation of yeasts and the direct identifi
Chromogenic medium for the selective isolation of yeasts and the direct identification of Candida albicans
Selective and differential chromogenic medium for screening of rectal swabs for
Selective and differential chromogenic medium for screening of rectal swabs for carbapenemase-producing Escherichia coli and Klebsiella pneumoniae.
JSO
CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, EXCLUDING MUELLER HINTON AGAR
API 50 CHL Medium, for ID of Lactobacillus and related genera, is a ready-to-use
API 50 CHL Medium, for ID of Lactobacillus and related genera, is a ready-to-use allowing fermentation of the 49 carbohydrates on the API 50 CH strip (Ref. 50 300).
API ® OF Medium enables lab personnel to differentiate oxidative or fermentative
API ® OF Medium enables lab personnel to differentiate oxidative or fermentative metabolism of glucose by bacteria. It is designed to be used with API 20 E strips.
The Serum free reagent can be used with VIDAS ® assays for which its use is clea
The Serum free reagent can be used with VIDAS ® assays for which its use is clearly indicated in the VIDAS assay package insert.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of antifungal.
Etest is a quantitative technique for determining susceptibility of antifungal. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of antifungal.
Etest is a quantitative technique for determining susceptibility of antifungal. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining the MIC of antimicrobial agent
Etest is a quantitative technique for determining the MIC of antimicrobial agents against microorganisms and for detection of resistance mechanisms.
The eMAG platform is intended for the automated isolation (purification and conc
The eMAG platform is intended for the automated isolation (purification and concentration) of total nucleic acids (RNA/DNA) from biological specimens. For in vitro diagnostic use
VIDAS® FSH (FSH) assay is a quantitative immunoassay intended for use on VIDAS f
VIDAS® FSH (FSH) assay is a quantitative immunoassay intended for use on VIDAS family instrument in the detection of FSH concentration in human serum or plasma
The VIDAS ® Lyme IgG and IgM assay for use on VIDAS family instruments for the
The VIDAS ® Lyme IgG and IgM assay for use on VIDAS family instruments for the presumptive detection of total antibodies (IgG/IgM) to Borrelia burgdorferi
TOXO IgG II (TXG) assay is a quantitative IA intended for use on VIDAS family i
TOXO IgG II (TXG) assay is a quantitative IA intended for use on VIDAS family instrument in the detection of anti - toxoplasma IgG concentration in human serum or plasma.
VIDAS ® CMV IgM (CMVM) assay is an automated qualitative IA intended for use on
VIDAS ® CMV IgM (CMVM) assay is an automated qualitative IA intended for use on VIDAS family instrument for detection of anti - CMV IgM antibodies in human serum.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
ETEST® is a manual, quantitative technique for determination of antimicrobial su
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 su
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 quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
The VITEK MS-CHCA matrix is used with the VITEK® MS System to enable identificat
The VITEK MS-CHCA matrix is used with the VITEK® MS System to enable identification of microorganisms. The matrix absorbs energy from the VITEK MS laser and transfers it to the microorganisms
PEX
System, Mass Spectrometry, Maldi Tof, Microorganism Identification, Cultured Isolates
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
Etest is a quantitative technique for determining susceptibility of clinically s
Etest is a quantitative technique for determining susceptibility of clinically significant bacteria. It provides a gradient of 15 doubling dilutions for MIC determination.
The Access Hybritech PSA Sample Diluent is intended for use with the Access Hybr
The Access Hybritech PSA Sample Diluent is intended for use with the Access Hybritech PSA assay to dilute patient samples containing total prostate specific antigen (PSA) concentrations greater than the S5 calibrator.
The Access Hybritech PSA Calibrators are intended to calibrate the Access Hybrit
The Access Hybritech PSA Calibrators are intended to calibrate the Access Hybritech PSA assay for the quantitative determination of total prostate specific antigen (PSA) levels in human serum using the Access Immunoassay Systems.
The Access Hybritech PSA assay is a paramagnetic particle, chemiluminescent immu
The Access Hybritech PSA assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of total prostate specific antigen (PSA) levels in human serum using the Access Immunoassay Systems. This device is indicated for the measurement of serum PSA in conjunction with digital rectal examination (DRE) as an aid in the detection of prostate cancer in men aged 50 years or older. Prostate biopsy is required for the diagnosis of cancer. This device is further indicated for the serial measurement of PSA to aid in the prognosis and management of patients with prostate cancer.
VIDAS® TPSA is a In Vitro Diagnostic kit for the quantitative detection of total
VIDAS® TPSA is a In Vitro Diagnostic kit for the quantitative detection of total prostate specific antigen (PSA) in human serum, using an enzyme immunoassay (EIA) method.
Heterogeneous Immunoassay Module Total Prostate Specific Antigen Flex® reagent c
Heterogeneous Immunoassay Module Total Prostate Specific Antigen Flex® reagent cartridge 120 Test
Dimension® clinical chemistry system TPSA Flex® reagent cartridge