Bischoff & Bischoff GmbH |01.11.2019 - revision: 1
EN
27
26
Senio
| Rollator
Rollator |
Senio
Important! This is especially useful information on
a given subject.
Warning! These are especially safety-relevant
instructions. Follow the directions in the manual!
1. Introduction
Dear user,
By purchasing a B+B rollator, Rollators Senio you are now the owner of
a top-quality German product that is setting new standards in terms of
its variability. This instruction manual is intended to help you become
more familiar with the operation and use of the rollator.
Please read and follow the instruction manual carefully before using
your new rollator for the first time. The instruction manual is an integral
and necessary component of the product. Keep the instruction manual
where you can refer to it, and if you transfer the rollator to another user,
please provide the manual to the new owner.
For visually impaired users, this document is available as a PDF file at
our website www.bischoff-bischoff.com.
Any repairs and adjustments require special technical training and may
therefore only be carried out by authorized B+B dealers.
1.1. Signs and symbols
2. Important safety Instructions
2.1. General safety instructions
•
Max. load of Senio: 136 kg
•
Pinch risk! Be careful when folding up and unfolding the rollator.
Make sure that clothing and body parts are not pinched between
the folding parts of the rollator.
•
Observe the minimum insertion depth of the handholds.
•
Each brake affects only one wheel.
•
The basket can carry a weight of max. 5 kg.
•
Do not use aggressive or caustic detergents to clean the rollator!
•
Check that the rollator is fully intact each time before using it.
Check that the brake is working.
•
Have your mobility dealer check the brakes every six months!
•
The surfaces of the rollator can heat up when exposed to direct
sunlight. There is a risk of injury.
•
Reporting incidents. The operator or user must immediately report
1. any malfunction
2. any change to the features or performance as well as
3. any inaccuracies in the marking or operating instructions of
a medical device, which has or could have led to death or to a
serious deterioration of the health of a patient, an employee or a
third party, to the Federal Institute for Drugs and Medical Devices
(BfArM). This institute will immediately forward the notification
to the operator’s competent authority and also inform the
manufacturer and the manufacturer’s competent authority.
