Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Inst
Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems,Manual Antimicrobial Susceptibility Test Systems,Panels, Test, Susceptibility, Antimicrobial
Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Inst
Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems,Manual Antimicrobial Susceptibility Test Systems,Panels, Test, Susceptibility, Antimicrobial
Manual Antimicrobial Susceptibility Test Systems,Instrument For Auto Reader & In
Manual Antimicrobial Susceptibility Test Systems,Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems,Panels, Test, Susceptibility, Antimicrobial,Susceptibility Test Cards, Antimicrobial,Gram Negative Identification Panel
Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Pane
Gram Negative Identification Panel,Susceptibility Test Cards, Antimicrobial,Panels, Test, Susceptibility, Antimicrobial,Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems,Manual Antimicrobial Susceptibility Test Systems
The Access SARS-CoV-2 IgG II Calibrators are intended to calibrate the Access SA
The Access SARS-CoV-2 IgG II Calibrators are intended to calibrate the Access SARS-CoV-2 IgG II assay for the in vitro semi-quantitative and qualitative detection of SARS-CoV-2 IgG antibodies in human plasma (lithium heparin, dipotassium EDTA, tripotassium EDTA, and sodium citrate) for use on the Access Immunoassay Systems only.The Access SARS-CoV-2 IgG II calibrators are only for use under the Food and Drug Administration's Emergency Use Authorization.
The Access Toxo IgG QC is intended for monitoring system performance of the Acce
The Access Toxo IgG QC is intended for monitoring system performance of the Access Toxo IgG assay.
The Access CEA QC (BSA matrix) controls are intended for monitoring the system p
The Access CEA QC (BSA matrix) controls are intended for monitoring the system performance of immunoenzymatic procedures for the quantitative measurement of Carcinoembryonic Antigen (CEA) using Access CEA reagents.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
The BUN method used on the Dimension clinical chemistry system is an in vitro di
The BUN method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of urea nitrogen in serum, plasma and urine.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.
This product is intended for the quantitative in vitro determination of Urea in
This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine.