Mobius Mobility LLC 22007 Manuale Utente
ADVERSE EVENTS
REPORTING
REPORTING
If an event occurs while you are using your ibot
please contact (Customer Service Information
goes here). Please be prepared to provide as
much information as possible related to the
event. This will be a great help for us.
please contact (Customer Service Information
goes here). Please be prepared to provide as
much information as possible related to the
event. This will be a great help for us.
To increase the product quality and to ensure
that our device is safe through the whole life
cycle we need you to let us know if any
reportable event occurs.
that our device is safe through the whole life
cycle we need you to let us know if any
reportable event occurs.
To meet that requirement and to ensure that our
products remain safe in your hands we need your
assistance.
products remain safe in your hands we need your
assistance.
We hope you never need to use the information
on this page but if there is an event please
contact us.
on this page but if there is an event please
contact us.
The FDA encourages healthcare professionals,
patients, caregivers and consumers to submit
voluntary reports of significant adverse events or
product problems with medical products to
MedWatch, the FDA’s Safety Information and
Adverse Event Reporting Program or through the
MedWatcher mobile app.
patients, caregivers and consumers to submit
voluntary reports of significant adverse events or
product problems with medical products to
MedWatch, the FDA’s Safety Information and
Adverse Event Reporting Program or through the
MedWatcher mobile app.
In
d
ic
a
tio
n
s
F
o
r
U
s
e
16
DKPX-09006-001-Rev. 1.7