IONOMAT 1
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• For children, the treatment is the same, but it is necessary to respect the recommended
current values. We advise the presence of an adult during the treatment
13.3 Disposal
At the end of life, the device is to be placed in a suitable reprocessing center. Under no
circumstances should the device and disposable probe be disposed of with household waste or
disposed of in the environment.
Pursuant to European Directive 2002/96 / EC, this electrical appliance
must not be disposed of in household waste but must be brought to a
waste disposal facility for processing for recovery.
13.4 Electromagnetic Sensitivity
This device complies with the requirements of EN 60601-1-2 which describes electromagnetic
compatibility (EMC) requirements for medical devices. IONOMAT 1 requires precautions against
EMC.
Interference Hazards: The use of accessories, sensors and cables other than
those specified, with the exception of sensors and cables sold by the manufacturer as an
internal component replacement part, may lead to increased levels of interference.
emission or a decrease in immunity levels of IONOMAT 1.
Using IONOMAT next to other devices may cause interference. Especially in the vicinity of
RF communication with higher immunity levels than the values in Table 9 of EN 60601-1-
2.
13.5 Intended User Profile & User Environment
The device is intended to be used in an environment but medical and in patients' homes. It is
intended for several users:
• Practitioner (Dermatologist / Physiotherapist / Podiatrist): Person who is currently
using medical devices
• Patient: Person (> 7 years) using this medical device at home
13.6 Pictograms used on IONOMAT 1
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