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Introduction
Thank you for choosing the VERSA pelvis positioning system INSERTO which is a combination of
technology and experience in the development of positioning systems for disabled people.
"Inserto seats" pelvic positioning system, can simply be adapted to the user as needed.
"Inserto seats" pelvic positioning system can also be customised, molded, modified, in order to
be set up and prepared as from prescription to anatomy and morphology of the user through
the detection of its body mesurements, and direct trials so as to obtain a custom seat for the
perfect replication of its anatomic shapes for supporting or compensing its deformities, as well
as the body loads distribution.
The INSERTO range is adaptable to somatic growth and pathological changes. Their composition
makes them very comfortable, achieving optimal comfort with the maximum functionality by
offering high postural solution. The pelvis positioning system Inserto seat can be combi-
ned, by means of an adhesive gripping tape, to any supporting base and/or wheelchair
whether manual or powered, provided that the structure will host the positioning system
is solid enough to safely support the user during the use.
This manual is based upon the medical devices requirements of the 93/42/CEE directive.
It is an indispensable instrument for the knowledge of the procedures for safe and correct use
of the device.
All professionals and users are encouraged to carefully read the 'placing in service instructions'
with the express invitation to strictly follow the indicated procedure.
The initial commissioning operations, subsequent adjustments and special maintenance must be carried out exclusively by
the professional operator.
If an individual custom seat has been prepared and set up as prescribed, it can not be used by other user.
Any operation of removal, preparation or adjustment for the specific user, on the basis of a prescription, have to be performed
by a professional operator and those interventions get the device customised. The professional user has the charge and the
responsibility to guarantee the efficacy and the performances of the device.
The EC declaration of conformity refers only and exclusively to the medical device "as it is" as
prepared by the manufacturer, when it is not modified with respect to the standard configuration.
The EC label is on the last pages of this manual and on the bottom of each medical device.
The features of the device are described in the Technical sheet here attached. After consulting
this manual, for further details, please contact our Customer Service at the following number:
+39 0831 777840
In case of major emergencies out of working hours, please fax to the following number:
+39 0831 730739
INSTRUCTION MANUAL
Monday to Friday from
We will reply as soon as possible.
www.versainserto.com
9,00 to 13,00
and from
14,30 to 18,30.
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