This website uses cookies to ensure you get the best experience.
Ok
Leave feedback
The information which you give in completing this form will be forwarded to the designated party for its use and will not be provided by us to any other parties.
It must comply with the following important requirements:
It must produce ozone within a wide range of concentrations.
It must be capable of precise regulation of ozone outputs within the available range of concentrations at the least possible step.
It must have high accuracy in maintaining the set ozone concentration within the available range of concentrations, it must be tested by the manufacturer for accuracy in maintaining the set concentration; the attested accuracy must not decrease within the lifetime.
It must have an automated stabilization system of ozone/oxygen flow rate; it should be tested by the manufacturer for accuracy in maintaining the set ozone/oxygen flow rate.
It must ensure a strictly dose-dependent ozone therapy.
It must have a great operation resource (durability) of an ozonation (discharge) chamber employed (not less than 2 000 hours).
It must have a built-in protection system against failure due to incorrect operation.
It must generate pure (contaminant-free) medical ozone (an ozone/oxygen gas mixture) (guaranteed by the manufacturer).
All materials, which have contact with ozone, must be ozone-resistant.
It must be equipped with a built-in or remote catalytic destructor of ozone to avoid ozone leakage and to ensure no inhalative exposure of ozone to the patient and medical personnel since ozone is a toxic gas and irritates respiratory epithelium.
It must come with a full range of ozone-resistant accessories.
It must come with good technical support (warranty and post-warranty servicing).
It must be registered in the local MOH as a medical device.
It must be supported and recommended by the National or International Association of Ozone Therapy.