Since routinely screening of newborns for cystic fibrosis leads to early diagnosis, this means treatment can begin IMMEDIATELY! 

LeanGene partners with ELITech Group to provide the Jordanian market with the most accurate and reliable sweat collection and analysis systems.

ELITech Biomedical Systems is the acknowledged world leader for the laboratory diagnosis of cystic fibrosis with their proven Macroduct Sweat Collection System for stimulation and collection of sweat and the Sweat-Chek (total electrolyte analysis) or Chloro-Chek (Chloride titration) analyzers. When considering a potential laboratory diagnosis of cystic fibrosis, a physician still relies heavily upon the results of the sweat test, which is capable of producing an unequivocal, quantitative result to corroborate clinical observations. The Macroduct System provides the most accurate and simple sweat test system available. ELITech’s peerless scientific and engineering expertise has also produced Nanoduct, the completely integrated and miniaturized sweat analysis system for patients of any age. The Nanoduct patented in-situ stimulation and analysis provide clinicians with the earliest possible laboratory diagnosis of cystic fibrosis, enabling doctors to intervene and treat this disease in the earliest days of life.

Neonatal Sweat Analysis System

The Nanoduct® Neonatal Sweat Analysis System simplifies the sweat test and for the first time makes possible reliable laboratory diagnosis of cystic fibrosis in the first days of life.Nanpduct 2 The compact and ergonomic Nanduct® updates the classic method of inducing sweat by pilocarpine iontophoresis, followed by continuous-flow analysis using the unique Nanoduct sensor cell. Results appear quickly on the display.

Nanoduct has sensitive and robust self-diagnostics for complete monitoring of all system functions and now includes computer and printer interface capability. To record more detailed information or to capture the results in a computer file, Wescor’s Nanoduct Lab Report software for Windows® combines user-provided information with measurement results directly from the Nanoduct to a printable and/or savable report.

Nanoduct® Brochure

Chloridometer

ChloroChek® The perfect CF diagnostic companion to the Macroduct® Sweat Collection System.ChloroCheck 2

The ChloroChek Chloridometer was designed to work with the Macroduct Sweat Collection System for analyzing sweat chloride for the laboratory diagnosis of cystic fibrosis.

ChloroChek is easy to operate and gives results in less than 20 seconds. Simply pipette in a 10 microliter sample of sweat and get a results of the display instantly.

ChloroChek has an intuitive touch-screen interface with simple prompts and leads the operator through the entire process of measuring chloride levels of sweat samples.

CloroCheck® Brochure

Sweat Collection System

Standardized sweat testing for the laboratory diagnosis of cystic fibrosis.
Macroduct2The Macroduct® system is the Webster Sweat Inducer, and the Macroduct Sweat Collector. Together they have revolutionized the laboratory sweat test for cystic fibrosis, and have brought early intervention to thousands of CF patients around the world. The heart of this system is simplicity.

Also introducing the new FDA-cleared Macroduct® Advanced Sweat Collection System. Include a touch screen user interface with built in step-by-step graphic controlled instructions that further standardize pilocarpine iontophoresis and sweat collection for optimum results.

 

Total Electrolyte Analysis

Sweat-Chek™ Analyzer, a dedicated analyzer for the Macroduct System for total electrolyte analysis of sweat samples. Sweat Check 2

Interfacing perfectly with Macroduct, Sweat-Chek brings simplicity and economy to the analytical phase of the sweat test. A truly practical sweat testing system is now within the means of small hospitals, local clinics, or private practitioners.

While clinicians have traditionally used sweat chloride or sweat sodium ion assay, sweat conductivity is a proven method of sweat analysis. It is a simple and reliable indicator to confirm or exclude the physician’s clinical diagnosis of cystic fibrosis.

 

 

 

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