ACE Calibrator is intended to be used with Sentinel ACE Liquid Reagent for the p
ACE Calibrator is intended to be used with Sentinel ACE Liquid Reagent for the preparation of the calibration for the kinetic determination of angiotensin converting enzyme (ACE) assay in human serum or plasma. For In Vitro Diagnostic use.
The Albumin BCP (6x50 mL) assay is an in vitro diagnostic test used for the dete
The Albumin BCP (6x50 mL) assay is an in vitro diagnostic test used for the determination of albumin in human serum or plasma. The assay is intended for professional use only. For In Vitro Diagnostic use only.
The Albumin BCP (6x20 mL) assay is an in vitro diagnostic test used for the dete
The Albumin BCP (6x20 mL) assay is an in vitro diagnostic test used for the determination of albumin in human serum or plasma. The assay is intended for professional use only. For In Vitro Diagnostic use only.
Lipase NG OC CTRL 2 must be used only to verify the performance of the Lipase NG
Lipase NG OC CTRL 2 must be used only to verify the performance of the Lipase NG.Use the Control Material like the specimens, according to the indicated analytical procedure.
JJX
Single (Specified) Analyte Controls (Assayed And Unassayed)
The Lipase NG assay is an in vitro diagnostic test used for the determination on
The Lipase NG assay is an in vitro diagnostic test used for the determination on AU480 and AU680 automatic analyzers of the lipase activity in serum and plasma by kinetic colorimetric method. The assay is intended for professional use only.
Plasmaproteins Cal 3x must be used only for the calibration of the plasmaprotein
Plasmaproteins Cal 3x must be used only for the calibration of the plasmaproteins tests listed in the Assigned Concentrations Table (TcA) using immunoturbidimetric methods. Use the calibrator according to the indicated analytical procedure. For in vitro diagnostic use only.
The kit is intended for the quantitative determination of Alpha 1-Acid Glycoprot
The kit is intended for the quantitative determination of Alpha 1-Acid Glycoprotein (AGP) in serum and plasma by immunoturbidimetry. For In Vitro Diagnostic Use only.
LKL
Alpha-1-Acid-Glycoprotein, Antigen, Antiserum, Control
Plasmaproteins Cal 3x must be used only for the calibration of the plasmaprotein
Plasmaproteins Cal 3x must be used only for the calibration of the plasmaproteins tests with immunoturbidimetric method.Use the Calibrator according to the indicated analytical procedure.For professional use only. For in vitro diagnostics use
Immuno Control Set is for use in quality control by monitoring accuracy and prec
Immuno Control Set is for use in quality control by monitoring accuracy and precision for the quantitative method as specified in the assigned concentration Table.Use the Control Material like the specimens, according to the indicated analytical procedure.For professional use only. For In Vitro diagnostic use.
The Lipase NG OC assay is an in vitro diagnostic test used for the determination
The Lipase NG OC assay is an in vitro diagnostic test used for the determination of the Lipase activity in serum and plasma by kinetic colorimetric method. The assay is intended for professional use only. For In Vitro Diagnostic use.
ACE Liquid reagent is for use in the determination of Angiotensin converting enz
ACE Liquid reagent is for use in the determination of Angiotensin converting enzyme (ACE) activity in human serum or plasma.For In Vitro Diagnostic use.
Clin Chem Control 2 is for use in quality control by monitoring accuracy and pre
Clin Chem Control 2 is for use in quality control by monitoring accuracy and precision for the quantitative method as specified in the assigned concentration Table. Use the Control Material like the specimens, according to the indicated analytical procedure. For In Vitro Diagnostic use.
Lipase NG Cal must be used only for the calibration of Lipase NG kinetic colorim
Lipase NG Cal must be used only for the calibration of Lipase NG kinetic colorimetric direct determination.For In Vitro Diagnostic use only.
ACE Control Set is intended to be used with Sentinel ACE Liquid Reagent to monit
ACE Control Set is intended to be used with Sentinel ACE Liquid Reagent to monitor the accuracy and precision of the kinetic determination of angiotensin converting enzyme (ACE) assay in human serum or plasma. For In Vitro Diagnostic use.
JJX
Single (Specified) Analyte Controls (Assayed And Unassayed)
The Lipase Color Liquid is an In Vitro Diagnostic test used for the determinatio
The Lipase Color Liquid is an In Vitro Diagnostic test used for the determination of the lipase activity in serum and plasma by kinetic colorimetric method. The assay is intended for professional use only.
Lipase NG OC CTRL 1 must be used only to verify the performance of the Lipase NG
Lipase NG OC CTRL 1 must be used only to verify the performance of the Lipase NG.Use the Control Material like the specimens, according to the indicated analytical procedure.
JJX
Single (Specified) Analyte Controls (Assayed And Unassayed)
The Cholinesterase Liquid is an In Vitro Diagnostic test used for the determinat
The Cholinesterase Liquid is an In Vitro Diagnostic test used for the determination of the cholinesterase activity in serum and plasma by kinetic colorimetric method. The assay is intended for professional use only.
DLI
Acetylcholine Chloride, Specific Reagent For Pseudo Cholinesterase
The Lambda light chains assay is an in vitro diagnostic test used for the quanti
The Lambda light chains assay is an in vitro diagnostic test used for the quantitative determination of Immunoglobulin bound and free lambda light chains (LAMBDA) in serum and Li-heparin plasma by immunoturbidimetry. It is intended to measure Immunoglobulin Lambda light chains (bound and free) using Synchron LX20 and Unicel DxC 600 Systems.
Clin Chem Cal must be used only for the calibration of clinical chemistry tests.
Clin Chem Cal must be used only for the calibration of clinical chemistry tests. For in vitro diagnostic use only.
Clin Chem Control 1 is for use in quality control by monitoring accuracy and pre
Clin Chem Control 1 is for use in quality control by monitoring accuracy and precision for the quantitative method as specified in the assigned concentration Table. Use the Control Material like the specimens, according to the indicated analytical procedure. For In Vitro Diagnostic use.
Lipase NG OC Cal must be used only for the calibration of Lipase NG. For In Vitr
Lipase NG OC Cal must be used only for the calibration of Lipase NG. For In Vitro Diagnostic use.
The kit is intended for the quantitative determination of ceruloplasmin (CER) in
The kit is intended for the quantitative determination of ceruloplasmin (CER) in serum and plasma by immunoturbidimetry. For in vitro diagnostic use only.
The Kappa light chains assay is an in vitro diagnostic test used for the quantit
The Kappa light chains assay is an in vitro diagnostic test used for the quantitative determination of immunoglobulin bound and free kappa light chains (KAPPA) in serum and in Li-heparin plasma by immunoturbidimetry on Synchron LX20 and Unicel DxC 600 Systems.
The Ceruloplasmin assay is to be used for the quantitative immunoturbidimetric d
The Ceruloplasmin assay is to be used for the quantitative immunoturbidimetric determination of ceruloplasmin in serum and plasma. The assay is intended for professional use only. For In Vitro diagnostic use.
The Pancreatic Amylase assay is an in vitro diagnostic test used for the determi
The Pancreatic Amylase assay is an in vitro diagnostic test used for the determination on AU480, AU680 and AU5800 automatic analyzers of the pancreatic amylase in serum and plasma by enzymatic colorimetric method. The assay is intended for professional use only.
The CKMB UDR assay is an in vitro diagnostic test used for the kinetic quantitat
The CKMB UDR assay is an in vitro diagnostic test used for the kinetic quantitative determination on Unicel DxC600, DxC800 and Synchron LX20 systems of the CK-MB isoenzyme activity of creatine kinase in serum and Li-heparin plasma by inhibition method.
JHS
Differential Rate Kinetic Method, Cpk Or Isoenzymes
The CRP test system is intended for the quantitative in vitro determination of C
The CRP test system is intended for the quantitative in vitro determination of CRP concentration in serum.
The CRP test system is intended for the quantitative in vitro determination of C
The CRP test system is intended for the quantitative in vitro determination of CRP concentration in serum.
The device is intended for the quantitative in vitro diagnostic determination of
The device is intended for the quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum.
The CRP test system is intended for the quantitative in vitro determination of C
The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma.
The CRP test system is intended for the quantitative in vitro determination of C
The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma.
The CRP test system is intended for the quantitative in vitro determination of C
The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma.
The CRP test system is intended for the quantitative in vitro determination of C
The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma.
The CRP test system is intended for the quantitative in vitro determination of C
The CRP test system is intended for the quantitative in vitro determination of CRP concentration in serum.
The XCRP method used on the Dimension clinical chemistry system is an in vitro d
The XCRP method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of CRP in serum.
The device is a latex agglutination slide test intended for qualitative and semi
The device is a latex agglutination slide test intended for qualitative and semi-quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum.
The device is intended for the quantitative in vitro diagnostic determination of
The device is intended for the quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum.
The device is a latex agglutination slide test intended for qualitative and semi
The device is a latex agglutination slide test intended for qualitative and semi-quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum.
BioCheck HS-CRP ELISA Kit is intended for the quantitative determination of C-Re
BioCheck HS-CRP ELISA Kit is intended for the quantitative determination of C-Reactive Protein (CRP) in human serum.
The C-Reactive Protein HS ELISA is intended for the quantitative determination o
The C-Reactive Protein HS ELISA is intended for the quantitative determination of C-reactive protein (CRP) in human serum.Enhanced sensitivity measurements of CRP can be useful for the detection and evaluation of infection, tissue injury, inflammatory disorders and associated diseases.
For use as a consistent test sample of known concentration for monitoring assay
For use as a consistent test sample of known concentration for monitoring assay conditions for C-reactive protein (CRP).
For the quantitative determination of human C-reactive protein (CRP) in serum an
For the quantitative determination of human C-reactive protein (CRP) in serum and plasma by immunoturbidimetric assay.
For the quantitative determination of human C-reactive protein (CRP) in serum an
For the quantitative determination of human C-reactive protein (CRP) in serum and plasma by immunoturbidimetric assay.
For the quantitative determination of human C-reactive protein (CRP) in serum by
For the quantitative determination of human C-reactive protein (CRP) in serum by immunoturbidimetric assay.
For the quantitative determination of human C-reactive protein (CRP) in serum by
For the quantitative determination of human C-reactive protein (CRP) in serum by immunoturbidimetric assay.
These CRP Controls Set are intended for use in CRP test systems to validate perf
These CRP Controls Set are intended for use in CRP test systems to validate performance of the assay. The controls may also be useful in assessing test precision or analytical errors.2 For in vitro diagnostic use only. C-reactive protein (CRP) is described in the literature as an acute phase protein that is involved in the activation of complement, acceleration of phagocytosis, and detoxification of substances released from damaged tissue. CRP is one of the most sensitive indicators of inflammation.
The CRP Calibrator Set is intended to be used for the calibration of the CDS CRP
The CRP Calibrator Set is intended to be used for the calibration of the CDS CRP Reagents. For in vitro diagnostic use only. The calibrators in this kit contain known quantities of human C-reactive protein. These reagents are to be used as calibrators with the manufacturer’s CRP Reagents.
For the quantitative determination of C-reactive protein in serum or plasma by l
For the quantitative determination of C-reactive protein in serum or plasma by latex particle enhanced immunoturbidimetric assay. For in vitro diagnostic use only. C-reactive protein (CRP) is an acute phase protein that is involved in the activation of complement, acceleration of phagocytosis, and detoxification of substances released from damaged tissue. As such, CRP is considered to be one of the most sensitive indicators of inflammation.
Pointe CRP Reagent packaged for use on the Mindray BA800. 4 x 60ml R1, 4 x 60m
Pointe CRP Reagent packaged for use on the Mindray BA800. 4 x 60ml R1, 4 x 60ml R2. For the quantitative determination of C-reactive protein in serum or plasma by latex particle enhanced immunoturbidimetric assay. For in vitro diagnostic use only.
Pointe CRP Reagent 4 x 60ml R1, 4 x 60ml R2. For the quantitative determinatio
Pointe CRP Reagent 4 x 60ml R1, 4 x 60ml R2. For the quantitative determination of C-reactive protein in serum or plasma by latex particle enhanced immunoturbidimetric assay using the Mindray BS-480 analyzer.