Rehaforum MEDICAL Actimo Liberty Instrucciones De Uso página 11

Service life
If the rollator is used for its intended purpose and is cared for, checked and maintained in accordance with the in-
structions, a service life of five years can be assumed. However, the service life can vary considerably depending on
how the product is handled and cared for. For example, particularly careful handling of the product can extend the
service life, while extreme and improper handling of the product can shorten the service life.
The determination of the service life by Rehaforum Medical GmbH does not constitute an additional guarantee.
Disposal
Do not dispose of the rollator with normal household waste. Please contact your specialist dealer or take the rollator
to your local waste disposal centre.
Storage
Protect the rollator from dust and moisture and store it in a safe place to protect the frame and wheels from damage!
Protect your rollator from strong heat sources.
Technical data
Weight including bag and backrest: 6.9 kg
Weight without bag and backrest: 6.0 kg
Width: 65cm
Depth: 70cm
Height: 75.5 - 93 cm
Seat width: 44 cm
Seat depth: 20 cm
Seat height: 55 cm
Backrest height: 63 - 81 cm
Width between the handles (center line): 50 cm
Max. turning diameter: 88.5 cm
Recommended height: 160 - 190 cm
Folded size: 70cm x 25cm x 78cm
Wheel diameter: 20 cm
Wheel Thickness: 3.6cm
Max. loading bag: 5 kg
Max. load capacity: 136 kg
Frame material: Anodized aluminum (not susceptible to corrosion)
Material wheels: PU
Material handles: TPR
Seat/Pocket/Backrest: Oxford cloth
Warranty
The warranty period is 24 months and applies to all product defects that are demonstrably attributable to
manufacturing or material defects. Excluded from the warranty are Damage caused by natural wear and tear or
intent. Furthermore, the warranty does not cover damage caused by incorrect cleaning and care products or damage
caused by negligent or improper operation or use.
Notification/incident
All serious incidents occurring in connection with the product must be reported to the manufacturer and the
competent authority of the member state in which the user and/or patient is established.
Revision 2023/12 11