Cystic Fibrosis - Children
The only salt inhaler with controlled emission of aerosols for the treatment of respiratory diseases.
Cystic Fibrosisis a hereditary disease that manifests itself through an increased consistency of the mucous secretions of the body. The secretion may be dry and 'glue-like'. Cystic Fibrosis affects many organs, including the lungs and pancreas.

At a pulmonary level, chronic obstruction of the airways appears due to viscous mucus secretions. This favours bacterial colonisation which produces persistent infections.

On a pulmonary level Cystic fibrosis demonstrates:
- Persistent cough
- Difficulties in breathing
- Frequent respiratory infection
Added to the treatment recommended by the medical practitioner, the SaltMed saline inhaler may help to ensure the following through the controlled emission of dry, saline particles:
- Amelioration of cough due to the fluidisation of mucus and its easier elimination
- Improvement of breathing and an increase in physical effort capacity
- Increased resistance to respiratory infections through an improvement in localised immunity and the elimination of the pathogenic micro-organisms (i.e. bactericidal and bacteriostatic effects)
Instructions for use Benefits Techonology Certification Halotherapy F.A.Q.
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