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LORI Stander edition 2
CAUTION!
THIS SYMBOL IS USED TO STRENGTHEN THE FOCUS OF THE READER ON THE
CONTENT MARKED WITH THIS SYMBOL. FAILURE TO COMPLY WITH THE CONTENT
UNDER THIS SYMBOL MAY ENDANGER THE LIFE OR HEALTH OF THE USER.
2.
Identification of symbols
Manufacturer name and production date
Serial number
Permitted user weight
Avoid contact with water
Follow the user manual
The arrow indicates the discussed element
Arrows indicating the direction of movement
Conformity marking according to the Council Directive
93/42/EEC concerning medical devices, annex VII
3.
Compliance with requirements concerning medical devices
LORI Stander device meets the essential requirements of the MDD Directive 93/42/EEC for medical devices.
According to annex IX to the MDD Directive 93/42/EEC, the LORI Stander device is classified as a non-invasive, active class I
medical device in accordance with rule 1.
Conformity declaration of the device can be obtained in the Sales Department of the manufacturer.
CAUTION!
In case of any modification of the device, the use of non-original spare parts
or use with products of another manufacturer, the CE marking must be removed.
4.
Indications for using the device
LORI Stander can be used in persons with posture defects and muscle dysfunction. It is the perfect solution for children
suffering from cerebral palsy, muscular dystrophy, in various types of paralyses, tetraplegias and paraplegias, as well as for children
with posture disorders. This device may also be used for therapeutic and prophylactic reasons, as it can prevent the inevitable
consequences of paediatric diseases (incorrect posture and related disorders).
Obtaining a vertical position allows to improve the functioning of
patient’s
systems and organs, in particular:
−
cardiovascular system,
−
respiratory system,
−
digestive system,
−
skeletal system.
Using the device during the rehabilitation process of the patient increases the chances of recovery.