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Legal Information - Ottobock Motus CV Gebrauchsanweisung

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General information
• Loss of limbs
• Defective or deformed limbs
• Joint contractures or defects
• Muscle and nerve disorders
• Diseases such as cardiac or circulatory insufficiency, balance disorders or cachexia as well
as for geriatric patients who still have usable residual strength in the upper limbs.
The Motus was specially designed for individuals who are able to independently move in a
wheelchair.
Fitting considerations:
• Body size and body weight
• Physical and psychological limitations
• Age of the user
• Home and living conditions, and
• Environment.

1.4 Legal information

All legal conditions are subject to the respective national laws of the country of use and may
vary accordingly.
1.4.1 Service Life
Expected service life: 4 years.
The design, manufacturing and requirements for the intended use of the product are based on
the expected service life. These also include the requirements for maintenance, ensuring effec-
tiveness and the safety of the product.
Using the product beyond the specified expected service life leads to increased residual risk
and should only take place subject to the due diligence and deliberations of qualified personnel.
If the service life is reached, the user or a responsible attendant should contact the qualified
personnel who fitted the product or the manufacturer's servicing department . Here the user
can obtain information about known risks and the current options for refurbishing the product.
1.4.2 Liability
The manufacturer will only assume liability if the product is used in accordance with the descrip-
tions and instructions provided in this document. The manufacturer will not assume liability for
damage caused by disregard of this document, particularly due to improper use or unauthorised
modification of the product.
1.4.3 CE conformity
This product meets the requirements of the European Directive 93 / 42 / EEC for medical devices.
This product has been classified as a class I device according to the classification criteria
outlined in Annex IX of the directive. The declaration of conformity was therefore created by the
manufacturer with sole responsibility according to Annex VII of the directive.
44 | Ottobock
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