Cystic Fibrosis Equipment In Europe
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Manufactured by Lamellar Biomedical Ltdbased in UNITED KINGDOM
Cystic Fibrosis is a recessive chronic progressive genetic disorder of the lung with high morbidity and shortened life expectancy. The condition occurs as a consequence of differing hereditary mutations in the gene encoding for the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein, leading to mucus accumulation. ...
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Manufactured by Yourgene Healthbased in UNITED KINGDOM
Since the discovery of the CFTR gene in 1989, more than 1900 mutations and variants have been described. Many of these mutations are ‘private’, having been described only in one patient and/or family. Routine testing for all possible mutations is neither feasible nor cost effective and is therefore confined to testing for the most common ...
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Manufactured by Galapagos NVbased in BELGIUM
GLPG2737 is a Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) inhibitor which was observed to be well tolerated by patients in previous clinical trials. It is hypothesized that inhibition of the CFTR channel might reduce cyst growth and enlargement for patients with autosomal dominant polycystic kidney disease (ADPKD). In December ...
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Manufactured by Advanced Molecular Diagnosticsbased in UNITED KINGDOM
More than 1,000 mutations in the CFTR gene have been associated with cystic fibrosis. Most of these mutations in the CFTR gene change the production, structure, or stability of the chloride channel. All of these charevent the channel from functioning properly, which impairs the transport of chloride ions and the movement of water into and ...
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based in UNITED KINGDOM
are visualised as green amplicon peaks. The internal amplification control markers (non-cystic fibrosis) found in CF-EU2v1 are also included in the CF Italia Panel mix. These are visualised as red amplicon peaks and are used to monitor the efficiency of sample amplification and aid patient identification when running the CF Italia Panel alongside the ...
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based in UNITED KINGDOM
In 2016 the GBA legislated that a third tier of analysis (DNA testing) will be added to the current IRT/PAP protocol for Cystic Fibrosis newborn screening. The Elucigene CF DE kit uses fluorescent ARMS (Amplification Refractory Mutation System) allele specific technology to detect the 31 mandatory mutations required for newborn screening of ...
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Manufactured by ELITechGroupbased in FRANCE
ChloroChek The perfect CF diagnostic companion to the Macroduct Sweat Collection System. 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 ...
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Manufactured by ELITechGroupbased in FRANCE
Standardized sweat testing for the laboratory diagnosis of cystic fibrosis. The 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 ...
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Manufactured by TEM-SEGAbased in FRANCE
The Dopplex DMX is the perfect vascular assessment tool. It provides a bidirectional curve which is only generated from the digital doppler spectrum. This gives the clinician objective evidence to aid in the diagnosis of vascular disease that other dopplers may find difficult or impossible to perform. Its algorithms optimize the presentation of curves and improve sound quality using our ...
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Manufactured by Oasis Diagnosticsbased in USA
Oasis Diagnostics Corporation offers 2 kits for the detection of Cystic Fibrosis (CF). The CF StripAssay is a cost effective tool for identifying gene mutations indicative of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). The CF StripAssay TUR is a kit that specifically identifies mutations present in the ...
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Manufactured by PhysioAssistbased in FRANCE
The SIMEOX therapy provides effective and comfortable airway clearance for patients suffering from chronic lung diseases (such as Cystic Fibrosis, Bronchiectasis, COPD) having lung congestion and difficulties to mobilize their ...
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Manufactured by PARI GmbHbased in UNITED KINGDOM
The PARI BOY Classic – The all-rounder for acute and chronic respiratory diseases from the age of 4. The PARI BOY Classic has a new, modern design, whilst retaining the superior efficiency customers expect from PARI. The PARI BOY Classic can be used to treat conditions such as COPD, bronchiectasis, asthma, cystic fibrosis and ...
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by Pureims B.V.based in NETHERLANDS
Colistin Cyclops™ is a pre-filled colistin dry powder inhaler for the treatment of pulmonary Pseudomonas aeruginosa infections in cystic fibrosis and bronchiectasis. It offers a more patient-friendly alternative to other methods of administering colistin, because it is easy to use, easy to carry, pre-filled and disposable (no ...
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Manufactured by Micrel Medical Devices SAbased in GREECE
Rythmic™ Evolution is an ambulatory pump for Acute and Chronic Pain management, as well as other continuous infusion therapies such as Chemotherapy, Cystic Fibrosis, Primary Pulmonary Hypertension, ...
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Manufactured by Yourgene Healthbased in UNITED KINGDOM
A single workflow solution for the molecular diagnosis of Male Factor Infertility, Y-chromosome microdeletion analysis, Extension analysis of microdeletions, Sex chromosome aneuploidy analysis, Investigation of Cystic Fibrosis related CBAVD. Identifying the genetic causes of male infertility can result in more effective clinical ...
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Manufactured by Epithelixbased in SWITZERLAND
Epithelix is offering primary Human Small Airway Epithelial Cells (hSAEC), passage 1, isolated from biopsies. They are commonly used for in vitro studies related with pulmonary diseases and chemical testing. They are now a standard for research on asthma, COPD, cancer, cystic fibrosis, bacterial and viral infections. These cells are also a ...
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Manufactured by Epithelixbased in SWITZERLAND
Epithelix is offering primary Human Airway Epithelial Cells, passage 1, isolated from biopsies : Nasal (hAECN); Tracheal (hAECT); Bronchial (hAECB). hAECB, hAECT and hAECN are commonly used for in vitro studies related with pulmonary diseases and chemical testing. They are now a standard for research on asthma, COPD, cancer, cystic ...
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Manufactured by CEGLA Medizintechnik GmbH & Co. KGbased in GERMANY
The only inhalation aid with a patented guardian angel concept! (Further development of the RC-Compact-Space-Chamber PLUS). Optimizes the effect of the medication for respiratory diseases such as bronchial asthma, bronchitis, COPD and cystic fibrosis and is a reliable companion for small and large patients. The inhalation aid is ...
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Manufactured by Epithelixbased in SWITZERLAND
GENERAL FEATURES OF SMALLAIR™-HF: Reconstituted using primary small airways human cells; Ready and easy to use; Long ...
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Manufactured by Epithelixbased in SWITZERLAND
MucilAir™-HF is a version of MucilAir™ cocultured with human primary fibroblasts. Human Airway Epithelia consisting of primary epithelial cells (MucilAir™) cocultured with Human airway Fibroblasts (HF). ...
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