4
ENGLISH
To ensure safety for users, Moretti S.P.A. test and respect the EN ISO 10535:2006 specific
for lifters, to guarantee greater security.
5. GENERAL WARNINGS
WARNING!
Always pay close attention to the presence of moving parts that could cause limb
entrapment and injury.
• For proper use of the device refer to this manual, checking with a particular attention at
the warnings before use.
• For proper use of the device to consult your doctor or therapist.
• Keep the packaged product away from any source of heat because the packaging is made
of cardboard.
• The useful life of the accessory is determined by wear of parts that cannot be repaired
and/or replaced.
• Be careful when children are nearby.
• Do not exceed the maximum payload.
• The user and/or the patient will have to report any serious accident that have occurred
related the device to the manufacturer and appropriate authority of the State which the
user and/or patient belongs to.
6. SYMBOLS
Product code
Unique Device Identification
CE mark
EC
REP
0197
S N
Manufacturer
Batch Lot
Read the instruction manual
Medical Device
Conditions of disposal
EC
REP
0197
S N
Attention, should read the instructions
Production dates
EC
REP
0197
S N
Waste Electrical & Electronic Equipment (WEEE)
Protection against dust and water splashes
B Type
7. GENERAL DESCRIPTION
The ARKIMED patient lift helps users to move less self-sufficient. Ideal for wheelchair users. It
is the perfect aid to transfers the patient from a sitting or lying down. Facilitates the work of
medical staff while making patient transfers from one surface to another much safer, thanks to the
breadth and stability of the opening leg. Electric ARKIMED patient lift meets all requirements for
a comfortable and safe transfers, due to its unit control: it is an intelligent monitoring system that
means a bright code checks the charge level of the battery and the actuator piston conditions.
Содержание RI700C
Страница 16: ......
Страница 32: ......
Страница 33: ...MA RI700C_RI701_RI701C_RI703C_RI705_RI710_RI710C 02 A_ESP_07 2020 GR AS ARKIMED MANUAL DE INSTRUCCIONES ESPA OL...