Important Safety Warnings - Nuvoair AIR NEXT Manual Del Usuario

Some conditions may pose a
relative danger to a patient or
EN
affect the validity of spirometry
performance and results. These
include, but are not limited to the
following: unstable cardiovascular
status, unstable angina, recent
myocardial infarction (within one
month) or pulmonary embolism,
haemoptysis of unknown origin,
recent pneumothorax, thoracic,
abdominal or cerebral aneurysms,
recent thoracic, abdominal or eye
surgery, acute disorders such
as nausea or vomiting, severe
respiratory distress, physical
limitations, cognitive impairment,
dementia.

IMPORTANT SAFETY WARNINGS

Air Next should never be used with
a charging phone. Make sure the
phone is unplugged before con-
ducting a spirometry test. Don't
use the device with a connected
AC/DC adaptor.
Once removed from its packaging,
check that there is no visible dam-
age on the device. In the case of
damage do not use it and return it
to the seller.
Air Next has been examined by an
independent laboratory which has
certified the conformity of the device
to the European Safety Standards
EN 60601-1 and guarantees the
EMC Requirements within the lim-
its set in the European Standard
EN 60601-1-2 and ETSI's
EN 300 328. It is a medical device
class IIa ("two a") product. Air Next
is constantly controlled during its
production, therefore the product
conforms to the essential require-
ments set by the Council Directive
93/42/EEC for medical devices.
• Use only with iOS and Android
devices specified on our website
www.nuvoair.com.
• Use only in environments speci-
fied in this user manual.
• Do not expose to liquids.
8
• Air Next is not made with
natural rubber latex.
• Should you lose the battery
hatch with required and device
specific information on it, the
guarantee will no longer be valid
and NuvoAir cannot provide
further support or guarantee
the condition or functionality of
the product.
Explanation of the safety signs and
symbols marked on the device:
Manufacturer's name and address.
CE mark: indicates that the device
is certified that it conforms to the
0598
requirements of the 93/42/EEC
medical device directive.
IP classification: indicates that the
IP32
device is protected against solid
objects over 2.5 mm entering as well
as faling drops of water, if the case is
disposed up to 15° from vertical.
Waste electrical and electronic
equipment: Dispose accordingly.