01 IMPORTANT INFORMATION
GENERAL INFORMATION
Thank you for choosing a rollator from Rehaforum.
Please read the complete instructions for use carefully before instal-
ling, adjusting or using the rollator for the first time. This will provi-
de you with important information that will allow you to fully utilise
the technical advantages. In addition, you will receive information
that will ensure operational safety and the best possible mainte-
nance of your rollator. If you require further information about the
rollator, please contact your specialist dealer.
These instructions for use contain all the necessary information for
handling the rollator. Please keep them in a safe place so that they
are available for future reference.
PRODUCT LABELLING
Rehaforum Medical GmbH
1
Daimlerstr. 12 a, 25337 Elmshorn, Germany
info@rehaforum.com, www.rehaforum.com
2
Actimo
Home, schwarz | black
®
Ausschließlich für den Innenbereich | intended for indoor use
3
(21)YYYYPOXXXXXXXXX
4
12643364
5
4
041314
034745
1. manufacturer
|
2. article description
cel number
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5. EAN code
UDI-DI / GTIN, (21) serial number
protection symbol
|
8. observe instructions for use
medical device
|
10. dual system
10
|
REHAFORUM MEDICAL
YYYY-MM
5 kg
100 kg
(01)04041314034745
(21)YYYYPOXXXXXXXXX
6
|
3. serial number
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6. UDI = Unique Device Identifier, (01)
|
7. rain protection symbol / sun
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9. CE marking /
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11. max. load
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12. production date
INTENDED PURPOSE AND PRODUCT DESCRIPTION
The rollator is designed to support walking and maintain the activity
of persons with limited mobility. The rollator is intended for indoor
use only. The rollator has steerable front wheels, a tray and a net for
transporting utensils.
INDICATION
The use of the rollator is suitable for persons with
•
slight restriction of movement due to, for example, joint diseases
or after operations
•
slight loss of strength due to cardiovascular disease, for example
•
mild balance disorders
CONTRAINDICATION
The use of the rollator is not suitable for persons with
•
perceptual disorders
12
•
severe balance disorders
•
severe visual disturbances
11
•
joint damage to the arms
•
loss of limbs on both arms
10
9
8
7
DECLARATION OF CONFORMITY
Rehaforum Medical GmbH declares the conformity of this product in
accordance with EU Regulation 2017/745.
|
4. arti-