Clinical Chemistry

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Clinical Chemistry

RANDOX LABORATORIES LIMITED
CATALOG #	QTY	PRICE	DESCRIPTION
AP313	0	-	An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.
AP3802	0	-	An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.
AP3877	0	-	An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.
AP7927	0	-	An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.
AS101	0	-
AS1202	0	-	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AS1204	0	-	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AS1267	0	-	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AS147	0	-
AS2359	0	-	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AS2800	0	-	The AST method used on the Dimension® clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of aspartate aminotransferase activity in serum or plasma.
AS3804	0	-	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AS3876	0	-	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AS7905	0	-	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AS7938	0	-	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.
AU2352	0	-
AU2353	0	-
AY1580	0	-	The amylase test system is intended for the quantitative in vitro determination of Amylase in serum, plasma or urine.
AY1582	0	-	The amylase test system is intended for the quantitative in vitro determination of Amylase in serum, plasma or urine.
AY2811	0	-	The AMY method used on the Dimension® clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of amylase activity in serum, plasma and urine.
AY2862	0	-	A Pancreatic α‑Amylase test system is a device intended for the quantitative in vitro determination of Pancreatic α‑Amylase activity in serum, plasma or urine.
AY3805	0	-	An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine.
AY3855	0	-	A Pancreatic α‑Amylase test system is a device intended for the quantitative in vitro determination of Pancreatic α‑Amylase activity in serum, plasma or urine.
AY7931	0	-	An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine.
AY7932	0	-	An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, or urine.
AY7934	0	-	The device is intended for the quantitative in vitro determination of pancreatic α amylase in serum, plasma and urine.
AY9707	0	-	An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine.
BE454	0	-
BM1362	0	-
CA2390	0	-	The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine
CA2807	0	-	The calcium method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of calcium concentration in serum.
CA3871	0	-	The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine
CA590	0	-	The calcium test system is a device intended for the quantitative in vitro determination of calcium in serum, plasma or urine
CA7941	0	-	The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine
CAL2350	0	-	The device is intended for use as a calibrator in clinical chemistry assays. Randox calibration sera are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry assays on a wide range of automatic analyzers.
CAL2351	0	-	The device is intended for use as a calibrator in clinical chemistry assays. Randox calibration sera are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry assays on a wide range of automatic analyzers.
CD116	0	-	The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
CD127	0	-	The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
CD129	0	-	The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
CD7942	0	-	The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.
CF1500	0	-	This product is intended for in vitro diagnostic use, in the quality control of diagnostic methods using CSF as a sample on clinical chemistry systems. The CSF controls are for the control of accuracy.
CF1501	0	-	This product is intended for in vitro diagnostic use, in the quality control of diagnostic methods using CSF as a sample on clinical chemistry systems. The CSF controls are for the control of accuracy.
CH203	0	-
CH2655	0	-	Enzymatic Clearance assay for the in vitro quantitative determination of HDL-cholesterol in human serum and plasma.
CH2673	0	-	The device is intended for in vitro diagnostic use in the calibration of Randox HDL and LDL cholesterol clearance methods
CH3810	0	-	For the quantitative in vitro determination of cholesterol in serum and plasma.
CH3811	0	-	An HDL-cholesterol test system is a device intended for the quantitative in vitro determination of HDL-cholesterol concentration in human serum and plasma.
CH3841	0	-	In Vitro device for the quantitative determination of LDL-Cholesterol in serum and plasma.
CK110	0	-	The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.
CK113	0	-	The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.

19,621 Results

Results Per Page

Catalog #

AvailableQty

Starting At

Name

Company Name

Description

CK113

CK NAC

RANDOX LABORATORIES LIMITED

The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.

CK110

CK NAC

RANDOX LABORATORIES LIMITED

The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma.

CH3841

LDL

RANDOX LABORATORIES LIMITED

In Vitro device for the quantitative determination of LDL-Cholesterol in serum and plasma.

CH3811

HDL

RANDOX LABORATORIES LIMITED

An HDL-cholesterol test system is a device intended for the quantitative in vitro determination of HDL-cholesterol concentration in human serum and plasma.

CH3810

CHOL

RANDOX LABORATORIES LIMITED

For the quantitative in vitro determination of cholesterol in serum and plasma.

CH2673

D LDL/HDL CAL

RANDOX LABORATORIES LIMITED

The device is intended for in vitro diagnostic use in the calibration of Randox HDL and LDL cholesterol clearance methods

CH2655

DIRECT HDL-CHOLESTEROL (HDL)

RANDOX LABORATORIES LIMITED

Enzymatic Clearance assay for the in vitro quantitative determination of HDL-cholesterol in human serum and plasma.

CH203

HDL-CHOLESTEROL (HDL)

RANDOX LABORATORIES LIMITED

CF1501

CSF CONTROL - LEVEL 3 (CSF CONTROL 3)

RANDOX LABORATORIES LIMITED

This product is intended for in vitro diagnostic use, in the quality control of diagnostic methods using CSF as a sample on clinical chemistry systems. The CSF controls are for the control of accuracy.

CF1500

CSF CONTROL - LEVEL 2 (CSF CONTROL 2)

RANDOX LABORATORIES LIMITED

CD7942

CO2

RANDOX LABORATORIES LIMITED

The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.

CD129

CO2

RANDOX LABORATORIES LIMITED

The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.

CD127

CO2

RANDOX LABORATORIES LIMITED

The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.

CD116

CO2

RANDOX LABORATORIES LIMITED

The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma.

CAL2351

CAL 3

RANDOX LABORATORIES LIMITED

The device is intended for use as a calibrator in clinical chemistry assays. Randox calibration sera are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry assays on a wide range of automatic analyzers.

CAL2350

CAL 2

RANDOX LABORATORIES LIMITED

CA7941

RANDOX LABORATORIES LIMITED

The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine

CA590

RANDOX LABORATORIES LIMITED

The calcium test system is a device intended for the quantitative in vitro determination of calcium in serum, plasma or urine

CA3871

RANDOX LABORATORIES LIMITED

The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine

CA2807

RANDOX LABORATORIES LIMITED

The calcium method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of calcium concentration in serum.

CA2390

Calcium (Ca)

RANDOX LABORATORIES LIMITED

The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine

BM1362

BETA 2 MICROGLOBULIN CALIBRATOR (B2M CAL)

RANDOX LABORATORIES LIMITED

BE454

BILIRUBIN ELEVATED SERUM (BIL CONTROL H)

RANDOX LABORATORIES LIMITED

AY9707

AMY

RANDOX LABORATORIES LIMITED

An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine.

AY7934

P AMY

RANDOX LABORATORIES LIMITED

The device is intended for the quantitative in vitro determination of pancreatic α amylase in serum, plasma and urine.

AY7932

AMY

RANDOX LABORATORIES LIMITED

An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, or urine.

AY7931

AMY

RANDOX LABORATORIES LIMITED

An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine.

AY3855

P AMY

RANDOX LABORATORIES LIMITED

A Pancreatic α‑Amylase test system is a device intended for the quantitative in vitro determination of Pancreatic α‑Amylase activity in serum, plasma or urine.

AY3805

AMY

RANDOX LABORATORIES LIMITED

An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine.

AY2862

P AMY

RANDOX LABORATORIES LIMITED

A Pancreatic α‑Amylase test system is a device intended for the quantitative in vitro determination of Pancreatic α‑Amylase activity in serum, plasma or urine.

AY2811

AMY

RANDOX LABORATORIES LIMITED

The AMY method used on the Dimension® clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of amylase activity in serum, plasma and urine.

AY1582

AMY

RANDOX LABORATORIES LIMITED

The amylase test system is intended for the quantitative in vitro determination of Amylase in serum, plasma or urine.

AY1580

AMY

RANDOX LABORATORIES LIMITED

The amylase test system is intended for the quantitative in vitro determination of Amylase in serum, plasma or urine.

AU2353

ASSAYED URINE CONTROL - LEVEL 3 (URN ASY CONTROL 3)

RANDOX LABORATORIES LIMITED

AU2352

ASSAYED URINE CONTROL - LEVEL 2 (URN ASY CONTROL 2)

RANDOX LABORATORIES LIMITED

AS7938

AST

RANDOX LABORATORIES LIMITED

The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.

AS7905

AST

RANDOX LABORATORIES LIMITED

The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.

AS3876

AST

RANDOX LABORATORIES LIMITED

The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.

AS3804

AST

RANDOX LABORATORIES LIMITED

The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.

AS2800

AST

RANDOX LABORATORIES LIMITED

The AST method used on the Dimension® clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of aspartate aminotransferase activity in serum or plasma.

AS2359

AST

RANDOX LABORATORIES LIMITED

The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.

AS147

ASPARTATE AMINOTRANSFERASE (AST)

RANDOX LABORATORIES LIMITED

AS1267

AST

RANDOX LABORATORIES LIMITED

The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.

AS1204

AST

RANDOX LABORATORIES LIMITED

The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.

AS1202

AST

RANDOX LABORATORIES LIMITED

The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma.

AS101

ASPARTATE AMINOTRANSFERASE (AST)

RANDOX LABORATORIES LIMITED

AP7927

ALP

RANDOX LABORATORIES LIMITED

An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.

AP3877

ALP

RANDOX LABORATORIES LIMITED

An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.

AP3802

ALP

RANDOX LABORATORIES LIMITED

An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.

AP313

ALP

RANDOX LABORATORIES LIMITED

An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma.