4
Please read this rst!
We would be pleased to answer your questions and we
welcome your suggestions. We do, of course, provide
support in case of technical problems. Please contact
your local EMS service center.
We wish you lots of success!
About this Manual
Please note that the English version of this manual is the
source from which all translations are derived. In case of
any discrepancy, the binding version is the English text.
These operating instructions are to ensure the correct
installation and use of this product. Always keep these
instructions close at hand.
Please read these operating instructions carefully as
they explain important details and procedures. Please
pay special attention to the safety precautions.
Any serious incident that has occurred in relation to the
product should be reported to the manufacturer and the
competent authority of the member state in which the
user and/or patient is established.
To prevent injury to people and damage to property,
please follow the corresponding directives.
They are marked as indicated:
Warning:
A warning indicates a situation which, if not
avoided, could result in death or serious
injury.
Precaution:
A precaution indicates a situation which,
if not avoided, may result in minor or
moderate injury to the user or patient or
damage to the equipment of other property.
Note:
Useful additional information and hints.
Product description
The DOLORCLAST
®
Radial system generates clinically
therapeutic pressure pulses. The pressure pulses are
generated ballistically in the handpiece from a supply
of compressed air from integrated compressors in the
console. The pressure pulses are delivered to the patient
via the handpiece applicator. The device allows control
of the pressure from 1-4bar; frequency up to 25Hz and
the number of pulses for the treatment. Please note that
this device can only be used on the U.S. market.
Indications for Use
The DolorClast Radial is intended for relief of minor
muscle aches and pains, temporary increase in local
blood circulation, and activation of connective tissue.
Intended User
The device must be used by qualied health experts (such
as doctors and physiotherapists) in hospitals, clinics,
medical universities and physical therapists’ offices.
They must use this device by fully complying with their
respective country’s regulations, accident prevention
measures, and strictly follow these instructions for use.
No specic training other than initial professional training
is required to use this medical device.
The practitioner is responsible for performing the clinical
treatments and for any dangers that may arise due to a
lack of skill and/or training.
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