User's Manual

4
Users Guide
Caution should be used for patients with suspected or diagnosed
epilepsy.
Some patients may experience skin irritation or hypersensitivity due to
the electrical stimulation or electrical conductive medium. The irritation
can usually be reduced by using an alternate conductive medium or
alternate electrode placement.
Electrode placement and stimulation settings should be based on the
guidance of the prescribing practitioner.
The NESS L300™ should be used only with electrodes supplied by
NESS Ltd.
Specific physician clearance should be obtained prior to use in patients
with alteration of normal arterial or venous flow due to local insufficiency,
occlusion, arterio-venous fistula for the purpose of hemodialysis, or
primary disorder of the vasculature.
Specific physician clearance should be obtained when there is a structural
deformity or placement of metal implant in the area to be stimulated.
The safety of the NESS L300’s use during pregnancy has not been
established.
Skin problems in areas of contact with the Orthosis may be aggravated
by use of the NESS L300™.
The NESS L300™ should be turned off before removing or replacing the
electrodes.
The NESS L300™ should be kept out of the reach of children.
The NESS L300™ Control Unit is splash proof. However, it should be
protected from any contact with water such as dampness from sinks,
bathtubs and shower stalls, from weather such as rain or snow or any
other source of water.