p4
GoTo Seat User Manual
English
SECTION 02: Certification
The GoTo Seat is classified as a Class I Medical Device under EU and UK
regulations. As the manufacturer, James Leckey Design Limited, declares that
this product conforms to the Medical Device Regulation (2017/745), UK Medical
Device Regulations 2002, Medial Device Directive (93/42 EEC) and EN 12182:2012
Assistive products for persons with disability, general requirements and test
methods.
Notice to the user and/or patient: Any serious incident that has occurred
in relation to the device should be reported to the manufacturer and the
competent authority of the Member State in which the user and/or patient is
established.
NOTE:
General user advice.
Not following these instructions may result in physical injury, damage to the
product or damage to the environment!
SECTION 03: Warnings
and Cautions
Warning Toppling Hazard:
•
Always read user instructions fully
before use.
Warning Finger Trap Hazard:
•
Ensure that the user or carer does
not touch any moving joint or pivot
that is not locked.
•
While the user is in the product,
the carer should strive to keep
product adjustments to a
minimum.
Warning Occupant Security:
•
User transfers in and out of the
product must be done with
appropriate equipment and
personnel.
•
Ensure that all harnesses are
securely applied.
•
If the user exhibits any form of
distress, remove from the product
as quickly as is safely possible.
•
Users should not be left
unattended at any time whilst
using Leckey equipment.
