Empi 300PV Manual De Instrucciones página 15

Idiomas disponibles

Idiomas disponibles

If the device appears to be functioning, and there is no stimulation:
• Replace the lead wires and/or electrodes.
For more detailed Troubleshooting information, see Section 4.
2.5.3.2 Repair
There are no user serviceable parts inside the device. If the device appears to be
non-functional, contact your clinician, or contact Empi directly at (800) 328-2536.
2.5.4 Maintenance, Cleaning and Storage
2.5.4.1 Maintenance
Under normal conditions, the device does not require periodic maintenance,
calibration or testing.
2.5.4.2 Cleaning
Use a damp cloth with mild soap to clean the exterior of the device and lead
wires. Use of other cleaning solutions may damage these items. Never immerse
the device in liquids.
2.5.4.3 Storage
To store the stimulator for an extended time (more than 30 days), remove the
batteries and store the device in a cool and dry place.
3 Product Information (Clinician)
The Empi 300PV is a state-of-the-art NMES system that incorporates three
widely used clinical modalities: TENS, NMES and High Volt (HV). The device is
designed to allow the clinician to introduce electrotherapy into the rehabilitation
cycle earlier than with conventional NMES devices. The NMES component can
be used pre-surgically to treat disuse atrophy. The HV feature can be used pre-
or post-surgically to increase local circulation. The numerous NMES protocols
are available for muscle re-education when the patient is ready for the post-
surgical rehabilitation program. The 300 PV may also be used as a TENS for
the symptomatic relief and management of chronic, intractable pain and as an
adjunctive treatment for post-surgical and post-trauma acute pain.
The 300 PV has thirteen preprogrammed regimens for NMES, TENS, and HV,
or 3 available Sport PPR's, each with Empi recommended default settings. All
the clinician needs to do is choose the appropriate PPR for the intended clinical
application (see Section 3.2) and the device is ready for use. Additionally, the
clinician can control the patient's access to the treatment parameters by locking
the output. For treatment flexibility, multiple stimulation parameters are also
user adjustable including two independent intensity controls, discrete adjustable
rate settings, adjustable ON and OFF time controls and treatment duration time.
Stimulation may be synchronous or asynchronous. In addition, the device may be
set for either Symmetric, or Asymmetric Biphasic or Monophasic waveforms as
necessary.
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