The Actim PROM Controls kit consists of one of each of the following components:1. Actim PROM Negative Control (0 μg/L)2. Actim PROM Low Positive Control (40 μg/L)3. Actim PROM High Positive Control (250 μg/L)4. Actim Reconstitution Solution5. Instructions for use

Actim PROM test pouch. Each pouch includes:- One tube of Specimen Extraction Solution (0.5 mL). This phosphate-buffered solution contains bovine serum albumin (BSA), protease inhibitors and preservatives.- One dipstick in a sealed aluminum foil pouch with desiccant.- One sterile polyester swab for specimen collection.

QuikRead go® CRP Verification Set is designed to be used for calibration verification and for method validation of the QuikRead go® CRP system. It is intended for use with the QuikRead go® CRP test and the QuikRead go® instrument.

QuikRead go® CRP Control Set is intended for use as assayed quality-control material for monitoring the performance of the quantitative QuikRead go CRP assay with the QuikRead go Instrument.

QuikRead go® instrument has been designed to measure quantitative test results from patient samples using QuikRead go® reagent kits.

UniQ® PINP RIA is a quantitative radioimmunoassay designed for the measurement of the concentrationof intact aminoterminal propeptide of type I procollagen, an indicator of osteoblastic activity, in human serum.

Gastrin-17 Advanced test is an in vitro microplate-based quantitative enzyme-linked immunosorbent assay (ELISA) for the determination of human gastrin-17 (G-17) from EDTA plasma or serum samples. The test is intended to aid in diagnosing atrophic gastritis (AG) from patients with Helicobacter pylori infection or at risk to develop malignant cellular changes in stomach mucosa. In addition, the test aids in screening conditions that necessitate additional examination or treatment from healthy stomach mucosa as G-17 is a direct biomarker of antral structure and function, and an indirect biomarker of gastric corpus. Furthermore, Gastrin-17 Advanced test is intended for screening and monitoring the acid output of the stomach. The test can be conducted either manually or automatically and is to be used by healthcare professionals.

Clinical Chemistry Test Systems / Sodium test system. A sodium test system is a device intended to measure sodium in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of aldosteronism (excessive secretion of the hormone aldosterone), diabetes insipidus (chronic excretion of large amounts of dilute urine, accompanied by extreme thirst), adrenal hypertension, Addison's disease (caused by destruction of the adrenal glands), dehydration, inappropriate antidiuretic hormone secretion, or other diseases involving electrolyte imbalance.

Clinical Chemistry Test Systems / Potassium test system. A potassium test system is a device intended to measure potassium in serum, plasma, and urine. Measurements obtained by this device are used to monitor electrolyte balance in the diagnosis and treatment of diseases conditions characterized by low or high blood potassium levels.

Clinical Chemistry Test Systems / Chloride test system. A chloride test system is a device intended to measure the level of chloride in plasma, serum, sweat, and urine. Chloride measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders such as cystic fibrosis and diabetic acidosis.

A discrete photometric chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. This device is intended for use in conjunction with certain materials to measure a variety of analytes. Different models of the device incorporate various instrumentation such as micro analysis apparatus, double beam, single, or dual channel photometers, and bichromatic 2-wavelength photometers. Some models of the device may include reagent-containing components that may also serve as reaction units.

A discrete photometric chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. This device is intended for use in conjunction with certain materials to measure a variety of analytes. Different models of the device incorporate various instrumentation such as micro analysis apparatus, double beam, single, or dual channel photometers, and bichromatic 2-wavelength photometers. Some models of the device may include reagent-containing components that may also serve as reaction units.

A discrete photometric chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. This device is intended for use in conjunction with certain materials to measure a variety of analytes. Different models of the device incorporate various instrumentation such as micro analysis apparatus, double beam, single, or dual channel photometers, and bichromatic 2-wavelength photometers. Some models of the device may include reagent-containing components that may also serve as reaction units.

A discrete photometric chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. This device is intended for use in conjunction with certain materials to measure a variety of analytes. Different models of the device incorporate various instrumentation such as micro analysis apparatus, double beam, single, or dual channel photometers, and bichromatic 2-wavelength photometers. Some models of the device may include reagent-containing components that may also serve as reaction units.

A discrete photometric chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. This device is intended for use in conjunction with certain materials to measure a variety of analytes. Different models of the device incorporate various instrumentation such as micro analysis apparatus, double beam, single, or dual channel photometers, and bichromatic 2-wavelength photometers. Some models of the device may include reagent-containing components that may also serve as reaction units.

A discrete photometric chemistry analyzer for clinical use is a device intended to duplicate manual analytical procedures by performing automatically various steps such as pipetting, preparing filtrates, heating, and measuring color intensity. This device is intended for use in conjunction with certain materials to measure a variety of analytes. Different models of the device incorporate various instrumentation such as micro analysis apparatus, double beam, single, or dual channel photometers, and bichromatic 2-wavelength photometers. Some models of the device may include reagent-containing components that may also serve as reaction units.

Used with 1235-501 AutoDELFIA® Plate Processor System or 1235-514 Fully Automatic DELFIA® System

1296-004 DELFIA® Plateshake is intended to be used with DELFIA reagents but can also be used for other applications where shaking of microtitration plates is required. One to four plates can be on the shaker simultaneously.

1296-026 DELFIA Platewash is a washer designed for automatic washing of microtitration strips or plates. It is self-contained, having built-in pumps for vacuum and dispensing and supplied with all the bottles and tubing needed for operation. For use with DELFIA analytes, ready-made programs are accessible.

Dried Blood Spot Puncher for DELFIA tests performed on filter paper in microplate format.

Used with 1235-514 Fully Automatic DELFIA® System

VICTOR2 D will primarly be used for measuring test kits supplied by Wallac especially for neonatal tests. Secondly VICTOR2 D can also be used for other measurements of TRF and prompt fluorescence. The user is a laboratory running screening on newborns or a general clinical chemistry lab running different hormones on blood samples.

VICTOR2 D will primarly be used for measuring test kits supplied by Wallac especially for neonatal tests. Secondly VICTOR2 D can also be used for other measurements of TRF and prompt fluorescence. The user is a laboratory running screening on newborns or a general clinical chemistry lab running different hormones on blood samples.

For the semi-quantitative determination of biotinidase in dried blood. Note: Kit contains multiple packages.

For the semi-quantitative determination of biotinidase in dried blood. Note: Kit contains multiple packages.

For the quantitative determination of amino acid, acylcarnitine and free carnitine concentrations in dried blood.

For the quantitative determination of galactose and galactose-1-phosphate in dried blood. Note: Kit contains multiple packages.

The product is to be used together with the NeoGram Amino Acids and Acylcarnitines Tandem Mass Spectrometry kit, and is intended for the measurement of amino acid, free carnitine, and acylcarnitine concentrations from newborn heel prick blood samples dried on filter paper.

Specimen Gate® PatientCare™ is intended for management of the follow-up workflow of a screening system.

Specimen Gate® Laboratory is a modular laboratory information management system intended for use as a calculator/data processing software for the storage, retrieval, and processing of laboratory data in newborn screening laboratories.

Time-resolved fluoroimmunoassay for the quantitative determination of human chorionic gonadotropin (hCG).

Time-resolved fluoroimmunoassay for the quantitative determination of human follicle stimulating hormone (hFSH).

Time-resolved fluoroimmunoassay for the quantitative determination of human luteinizing hormone (hLH).

Time-resolved fluoroimmunoassay for the quantitative determination of human thyrotropin (thyroid stimulating hormone - hTSH) in dried blood.

Time-resolved fluoroimmunoassay for the quantitative determination of thyroxine (T4) in dried blood.

Time-resolved fluoroimmunoassay for the quantitative determination of human chorionic gonadotropin (hCG).

Time-resolved fluoroimmunoassay for the quantitative determination of human chorionic gonadotropin (hCG).

For the quantitative determination of 17α-OH-progesterone (17-OHP) in dried blood.

For the quantitative determination of 17α-OH-progesterone (17-OHP) in dried blood.

For the quantitative determination of 17α-OH-progesterone (17-OHP) in dried blood.

Time-resolved fluoroimmunoassay for the quantitative determination of human thyrotropin (thyroid stimulating hormone - hTSH) in dried blood.

Time-resolved fluoroimmunoassay for the quantitative determination of human thyrotropin (thyroid stimulating hormone - hTSH) in dried blood.

Time-resolved fluoroimmunoassay for the quantitative determination of thyroxine (T4) in dried blood.

Time-resolved fluoroimmunoassay for the quantitative determination of thyroxine (T4) in dried blood.

Time-resolved fluoroimmunoassay for the quantitative determination of unconjugated estriol (uE3).

Time-resolved fluoroimmunoassay for the quantitative determination of unconjugated estriol (uE3).

For the quantitative determination of GALT (galactose-1-phosphate uridyl transferase) in dried blood. Note: Kit contains multiple packages.

For the quantitative determination of GALT (galactose-1-phosphate uridyl transferase) in dried blood. Note: Kit contains multiple packages.

For the quantitative determination of phenylalanine in dried blood.

For the quantitative determination of phenylalanine in dried blood.