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Idiomas disponibles
Technical data
Weight with armrests without bag: 9.1 kg; with bag: 9.5 kg
Tube diameter (oval): Width approx. 1 cm, length: 4.5 cm
Seat width: 46 cm
Seat depth: 23 cm
Seat height: approx. 61 cm
Adjustable height of forearm rest: 102 - 114 cm (in 7 steps)
Distance of the arm rests to the handle: 7-19 cm (in 5 steps)
Total length of armrest frame: 38 - 51 cm
Length of the arm rests: approx. 17 cm
Width between the forearm rests: 50 cm
Total length: approx. 76 cm
Total width: 68.5 cm
Overall height: 112.5 - 118 cm
Turning circle: 168 cm
Tyres front: 10"
Tyres rear: 8"
Tyre width: approx. 3 cm
Materials frame: anodised aluminium
Material pads: PU (plastic)
Material handles and wheels: TPE (thermoplastic elastomers)
Maximum load of the bag: 10 kg
Maximum load capacity: 136 kg
Recommended body height: approx. 1.65 - 1.90 m
Storage
Protect the rollator from dust and moisture and store it in a safe place to protect the linkage
and wheels from damage! Protect your rollator from strong sources of heat!
Disposal
Do not dispose of the rollator with normal household waste. Please contact your specialist
dealer or take the rollator to your local disposal point.
Service life
If the rollator is used within its intended purpose and is cared for, checked and maintained
according to the specifications, a service life of five years can be assumed for the Actimo®
Arthro. However, the service life can vary considerably depending on the treatment and care
of the product. For example, the service life can be extended by particularly careful handling
of the product, while the service life can be shortened by extreme and improper handling of
the product.
The determination of the service life by Rehaforum Medical GmbH does not constitute an ad-
ditional guarantee.
Warranty
The warranty period is 24 months and applies to all product defects that can be proven to be
due to manufacturing or material defects.
In particular, the warranty claim does not apply if the rollator has features that indicate repairs
or other interventions by unauthorised specialist dealers, or if third-party accessories have
been installed in the rollator without the prior written consent of Rehaforum Medical GmbH.
Notification / Incident
All serious incidents related to the device shall be reported to the manufacturer and to the
competent authority of the Member State in which the user and/or the patient is established.
Revision 08/2023
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