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2.1 Front and Rear panel:
1.5.3 Caution should be used in the presence of the following:
(a)When there is a tendency to hemorrhage following acute trauma or fracture
(b)Following recent surgical procedures when muscle contraction may disrupt the healing process.
(c)Over the menstruating or pregnant uterus
(d)Over areas of the skin which lack normal sensation.
1.5.4 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.
1.5.5 Electrode placement and stimulation settings should be based on the guidance of the prescribing
practitioner.
1.5.6 This device should be used only with the leads and electrodes recommended for use by the manufacturer.
1.5.7 Isolated cases of skin irritation may occur at the site of the electrode placement following long-term
application.
1.5.8 Effectiveness is highly dependent upon patient selection by a person qualified in the management of pain
patients.
1.5.9 If the stimulation levels are uncomfortable or become uncomfortable, reduce the stimulation amplitude to a
comfortable level and contact your physician if problems persist.
1.6 Adverse Reactions:
1.6.1 Possible skin irritation or electrode burn under the electrodes may occur.
1.6.2 Possible allergic skin reaction to tape or gel may occur.
2. PRODUCT DESCRIPTIONS
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Front View
Back View
Lateral View
Top View
Power Indicator Light
Low Battery Indicator Light
Amplitude
Control
Mode Selector
Amplitude Control
Rate Control
Electrode
Number
Selector
Slide Cover
Rate Control
Battery
Compartment
Amplitude
Control
Rate Control
Channel 1
Output
Receptacle
Channel 2
Output
Receptacle
Adaptor
Receptacle
Clip
