ASP motioncare LIANA, User Manual

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Gebrauchsanweisung LIANA
| Version 1.0
Seite 4 von 50
2. INTRODUCTION
2.1. Foreword
Correct use of the device is essential for operation. Therefore, read the supplied operating instructions carefully
and pay particular attention to the safety instructions.
Maintenance, testing, assembly, installations and all other technical interventions on the product may only be carried
out by motioncare or specialist companies authorised by motioncare. The operation of the product as well as
technical interventions on the product may only be carried out by instructed personnel.
ATTENTION
The operation of the product as well as technical interventions on the product may only be carried
out by instructed personnel.
The patient sitting/standing stabilisation aid LIANA is a medical device class 1 according to DIN EN 60601-1/IEC
60601-1 and DIN EN 60601-1-2/IEC 60601-1-2 as well as MDR Medical Device Regulation (EU) 2017/745. The
product is used to stabilise the patient at the edge of the bed as well as to stabilise the patient while they are
standing directly in front of the bed. LIANA is not suitable for patient transport.
If a serious incident occurs with a patient or user in connection with the use of the product or its accessories, contact
your dealer or the manufacturer. In the European Union, you are obliged to report serious incidents to the competent
authority of the respective member state. Other regulations may apply in other regions..
2.2. Liability and warranty
▪
Through the information in this manual, the manufacturer does not assume any liability for damage resulting
from improper use of the product. The product may only be operated by persons who are familiar with the
instructions, the product and the national laws, ordinances and regulations concerning work, safety and
accident prevention.
▪
The manufacturer of the product is only responsible for the safety and reliability of the product if regular
functional tests are carried out. Only operate the product with original accessories, otherwise any liability on
the part of the manufacturer will expire.
▪
In the event of technical interventions such as attachments or modifications to our products which are not
carried out by motioncare or a specialist company authorised by motioncare, any warranty for the
modifications and for the device or device function associated with the modification will expire.
▪
Any further liability of the manufacturer is excluded for damage resulting from the use of spare parts and
accessories not approved by the manufacturer.
▪
Slight deviations in the illustrations and explanations shown here from the actually delivered device are
possible for development reasons. Subject to technical changes and errors.
▪
The product is designed with type B applied parts. Here, all contactable, conductive parts are considered
applied parts.