Antar AT51036 - General Safety Warnings; Folding and Assembly Procedures; Handle Height Adjustment

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ENG
GENERAL WARNING
DO NOT assemble or use the product before reading and understanding these instruc ons. If you do not understand the warnings, cau ons or
instruc ons, contact your healthcare professional, distributor or technician before a emp ng to assemble the product to avoid injury or damage
to the product. Each user should ask their doctor or therapist to determine the appropriate adjustment op on and method of use. The rollator is
not intended to be steered by the user while si ng on it.
When adjus ng the height of the rollator, the doctor/therapist should be present to ensure that the user is supported and that the brakes are
correctly adjusted and the bolts  ghtened. When the rollator is extended, always make sure that the seat tube is locked and properly connected
to the frame and that the brake cable is inside the side tube and fi rmly a ached to it. Check the brake cable a er each height adjustment to
avoid the cable coming loose. Make sure that the knobs are locked so that the main support structure will not move as a result of pressure. The
quick release mechanism is fi  ed in the correct posi on and will remain in the release posi on even if pulled hard in the opposite direc on. The
copper pins in the adjustment tube extend from the right side. Failure to comply with the above may lead to injury. Before use, check that ALL
handle and seat adjustments have been secured and that the castors and moving parts of the product are in good condi on. During use ALL
castors must be in contact with the ground AT ALL TIMES to ensure the stability of the rollator. BEFORE the user sits on the seat, the brakes MUST
be in the locked posi on.
When the rollator is used in a sta onary posi on, its hand brakes MUST be in the locked posi on.
NOTE: Inspect all parts for damage that has occurred in transit. If such damage is observed, DO NOT use the product. Contact the manufacturer
for more informa on.
WARNINGS REGARDING FOLDING AND ASSEMBLY
A er unfolding or assembling the rollator, make sure the seat is locked into both tubes and both handle tubes are locked into the main support
frame with bolts and nuts. Also make sure that the copper pins slide out of the corresponding holes in the caster tubes and that they are properly
locked, and that both handles are at the same height and do not move.
UNFOLDING
Ensure that the seat tube is securely fastened in the locking mechanism, that all copper pins slide out of their respec ve holes, and that the front
and rear tubes are securely inserted into the main frame and secured with knobs. BEFORE use, always check that the rollator and its components
are securely locked in place. Then, screw in the screws to posi on the front wheels and also both tubes for the rear wheels.
FOLDING
Li the seat handle to fold the rollator as shown in fi g.5
Fig. 1 Fig. 2 Fig. 3 Fig. 4 Fig. 5
ADJUSTING THE HANDLE TUBE
Press the latch in the adjustment tube and move it up or down adjus ng the height. Make sure the latch is in the correct hole a er adjustment.
NOTE: When using and opera ng the rollator and when folding and adjus ng the mechanisms, there may be a risk of entrapment and/or
compression of body parts of the user/assisted person in the openings/gaps between the components. Take one handle and press down on the
seat un l all four pegs are unfolded and the seat is fl at. Perform these opera ons with par cular care. A er adjustment, stabilise the posi on by
carefully  ghtening the nuts/bolts.
WARNING:
In the event of a device-related “serious incident”, which directly or indirectly led to, could have led to, or is likely to lead to any of the following
events:
a)death of a pa ent, user or another person, or
b)temporary or permanent deteriora on of the health of a pa ent, user or another person, or
c)a serious risk to public health, such a “serious incident” must be no fi ed to the manufacturer and to the competent authority of the Member
State, in which the user or pa ent resides. For Poland, the competent authority is the Offi ce for Registra on of Medicinal Products, Medical
Devices and Biocidal Products.
WARNING:
In the event of pain, allergic reac ons or other alarming, unclear symptoms related to the use of the medical device, please consult a healthcare
professional.
NOTE: It is forbidden to use the product contrary to its intended use!
AT51036_ins_multi_002.indd 4T51036_ins_multi_002.indd 4 2022-12-02 10:10:002022-12-02 10:10:00