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.
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 device is an automated system, used for extraction and purification of nucle
The device is an automated system, used for extraction and purification of nucleic acid from clinical specimens.
Automated Nucleic Acids Extraction System ANDiS 360
A mains electricity (AC-powered) laboratory instrument intended to be used for t
A mains electricity (AC-powered) laboratory instrument intended to be used for the automated pre-analytical preparation of samples for downstream nucleic acid analysis. The instrument may be used to prepare various sample types through one or more pre-analytical steps which may include cell disruption, lysis, nucleic acid extraction, enzymatic digestion and/or nucleic acid purification. The device operates with minimal technician involvement and complete automation of all procedural steps.
Automated Nucleic Acids Extraction System ANDiS 350
The ReadiMag Pathogen Nucleic Acid Isolation Kit is a system that uses magnetic
The ReadiMag Pathogen Nucleic Acid Isolation Kit is a system that uses magnetic beads technology for isolation and purification of Pathogen nucleic acid from biological specimens. The purified nucleic acids can be directly used for the downstream tests. The product is intended to be used by professional users, such as technicians and physicians who are trained in molecular biological techniques.
96A Automated Viral DNA/RNA Isolation Kit is intended for isolation and purifica
96A Automated Viral DNA/RNA Isolation Kit is intended for isolation and purification of viral DNA and RNA from biological specimens (Nasopharyngeal Swabs, Oropharyngeal Swabs, Saliva and Cervical Swabs) by using automatic magnetic beads technology. The purified nucleic acids can be directly used for the downstream tests. The product is intended to be used by professional users, such as laboratory personnel who has been trained.
The 96B Automated Viral RNA Isolation Kit is a system that uses automatic magnet
The 96B Automated Viral RNA Isolation Kit is a system that uses automatic magnetic beads technology for isolation and purification of viral RNA from biological specimens (nasopharyngeal, oropharyngeal swabs or saliva). The purified nucleic acids can be directly used for the downstream tests. The product is intended to be used by professional users, such as technicians and physicians who are trained in molecular biological techniques.
32B Automated Viral RNA Isolation Kit is intended for isolation and purification
32B Automated Viral RNA Isolation Kit is intended for isolation and purification of viral RNA from biological specimens (nasopharyngeal, oropharyngeal swabs and saliva ) by using automatic magnetic beads technology, The purified nucleic acids can be directly used for the downstream tests. The product is intended to be used by professional users, such as laboratory personnel who has been trained.
96A Automated Viral DNA/RNA Isolation Kit is intended for isolation and purifica
96A Automated Viral DNA/RNA Isolation Kit is intended for isolation and purification of viral DNA and RNA from biological specimens by using automatic magnetic beads technology, The purified nucleic acids can be directly used for the downstream tests. The product is intended to be used by professional users, such as laboratory personnel who has been trained.
32A Automated Viral DNA/RNA Isolation Kit is intended for isolation and purifica
32A Automated Viral DNA/RNA Isolation Kit is intended for isolation and purification of viral DNA and RNA from biological specimens (nasopharyngeal, oropharyngeal swabs, saliva and cervical swabs) by using automatic magnetic beads technology, The purified nucleic acids can be directly used for the downstream tests. The product is intended to be used by professional users, such as laboratory personnel who has been trained.
The ReadiMag FFPE DNA Kit utilizes magnetic beads-based technology for isolation
The ReadiMag FFPE DNA Kit utilizes magnetic beads-based technology for isolation and purification of genomic DNA from formalin-fixed, paraffin-embedded (FFPE) biological specimens.
The ANDiS Viral Nucleic Acid Auto Extraction and Purification Pooling kit is a s
The ANDiS Viral Nucleic Acid Auto Extraction and Purification Pooling kit is a system that uses automatic magnetic beads technology for isolation and purification of viral RNA from biological specimens (nasopharyngeal, oropharyngeal swabs or anterior nasal swab). The purified nucleic acids can be directly used for the downstream tests. The product is intended to be used by professional users, such as technicians and physicians who are trained in molecular biological techniques.
ANDiS Viral Nucleic Acid Auto Extraction and Purification Pooling Kit
The 96A Automated Viral RNA Isolation Kit utilizes magnetic beads-based technolo
The 96A Automated Viral RNA Isolation Kit utilizes magnetic beads-based technology for automated isolation and purification of RNA from biological samples. The product is intended to be used by professional users that are trained in molecular biological techniques.
The Viral RNA Auto Extraction & Purification Kit utilize magnetic beads-based te
The Viral RNA Auto Extraction & Purification Kit utilize magnetic beads-based technology for automated isolation and purification of RNA from biological samples.The product is intended to be used by professional users that are trained in molecular biological techniques.
The ANDiS Viral RNA Auto Exttaction & Purification Kit is a system that uses au
The ANDiS Viral RNA Auto Exttaction & Purification Kit is a system that uses automatic magnetic beads technology for isolation and purification of viral RNA from biological specimens. The product is intended to be used by professional users, such as technicians and physicians who are trained in molecular biological techniques. The ANDiS Viral RNA Auto Extraction & Purification Kit is intennded for in vitro diagnostic use.
ANDiS Viral RNA Auto Extraction & Purification Kit
The chemagic 360-D is an automated laboratory instrument used in preanalytical p
The chemagic 360-D is an automated laboratory instrument used in preanalytical preparation of samples through magnetic particle separation technology for use with in vitro diagnostic clinical sample concentrating kits. The instrument is intended for use by healthcare professionals such as laboratory personnel or physicians who are trained in molecular biology techniques.
The chemagic Prepito-D is an automated laboratory instrument used in preanalytic
The chemagic Prepito-D is an automated laboratory instrument used in preanalytical preparation of samples through magnetic particle separation technology for use with in vitro diagnostic clinical sample concentrating kits. The instrument is intended for use by healthcare professionals such as laboratory personnel or physicians who are trained in molecular biology techniques.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It is particularly effective for the concentration of urine for the detection of Bence Jones proteinuria found in patients with myelomatosis.
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It is particularly effective for the concentration of urine for the detection of Bence Jones proteinuria found in patients with myelomatosis.
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It is particularly effective for the concentration of urine for the detection of Bence Jones proteinuria found in patients with myelomatosis.
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It is particularly effective for the concentration of urine for the detection of Bence Jones proteinuria found in patients with myelomatosis.
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It is particularly effective for the concentration of urine for the detection of Bence Jones proteinuria found in patients with myelomatosis.
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It
The Vivapore device is a single-use concentrator for in-vitro diagnostic use. It is particularly effective for the concentration of urine for the detection of Bence Jones proteinuria found in patients with myelomatosis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
This single-use device can be used for In Vitro Diagnostic applications, it is s
This single-use device can be used for In Vitro Diagnostic applications, it is suitable for use to concentrate or separate serum, urine, and other bodily fluids prior to further sample analysis.
MagXtract 3200 Automated Nucleic Acid Extraction SystemThe MagXtract 3200 system
MagXtract 3200 Automated Nucleic Acid Extraction SystemThe MagXtract 3200 system is an automated nucleic acid purification and PCR reaction preparation system consisting of MagXtract 3200 instrument, software and consumables. It must be used in combination with the authorized extraction kits which have been validated according to the IVD or other relevant regulations to perform the nucleic acid purifications. The MagXtract 3200 System is intended for use by professional users for the purification of nucleic acids and PCR sample prep from human samples for in vitro diagnostic purposes.Product Use Limitations:The MagXtract 3200 instrument is intended for indoor use only. The user is responsible for establishing performance characteristics necessary for downstream diagnostic applications. Appropriate controls must be included in any downstream diagnostic applications using nucleic acids, purified by the instruments.