NuvoAir ANMD01 Users Manual

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AIR NEXT USER MANUAL
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WHAT’S IN THE BOX
EN
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SETTING UP YOUR DEVICE
1 2 3
EN
Download the NuvoAir app from AppStore or Google Play Store.
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The spirometer lights up when it is connected to the mobile device.
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PERFORM A LUNG FUNCTION TEST
EN
1 2 3 4
Insert a new turbine by sliding it through the device.
Turn the turbine clockwise until it locks into place.
Create an account or sign in to an existing one and
select your prole.
4
Tap the plus button to perform a lung function test.
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PERFORM A LUNG FUNCTION TEST
5 6 7
Take a slow deep breath ­as deep as you can.
Close your lips around the opening of the turbine.
5
Blow as hard and as fast as you can into the mouthpiece.
Test
2s
Your exhalation should
exceed 6 seconds in order
to obtain a high quality test.
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PERFORM A LUNG FUNCTION TEST BATTERY
EN
CHECK
8 9 10
Test
6s
Keep going until you have completely emptied your lungs.
Results
You should rest 15 to 30 seconds before starting a new test.
Results
Flow
Volume
You can share
the test via e-mail.
Perform a minimum of 3 tests for high quality results. The app displays the best result.
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Battery: 100 %
Open app settings to check battery levels.
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INDICATIONS FOR USE
Air Next is intended to be used by:
• Healthcare professionals trained to perform spirometry tests on
patients of age ≥ 5 years old, > 10 kg and ≥ 110 cm.
• Adults trained by healthcare professionals (”competent adults”). Competent adult can assist a child
who is ≥5 years old, >10kg and ≥110 cm.
Air Next is intended to perform basic lung function and spirometry testing.
The actual diagnosis shall be done by a healthcare professional so home use is only for indicative purpose.
GENERAL INFORMATION
Air Next works with iOS and
Android devices and connects via bluetooth. Air Next is powered by 2 x 1.5 V AAA alkaline batteries. If the batteries are replaced or when
the device is discarded, dispose
the device as electronic waste.
Air Next is designed to work with single-use NuvoAir disposable turbines. When perform­ing a spirometry test, the user exhales into the turbine. The air­ow generated sets a rotor in mo­tion. Air Next registers the speed
of the spinning rotor, converts it
and transfers the data via Blue­tooth to the smartphone app.
LIMITATIONS OF USE &
CONTRAINDICATIONS
A spirometry test should only be
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carried out when the user is at rest (i.e. does not experience shortness
of breath) and in good health, and
thus in a suitable condition for the test.
An analysis of the results of a
spirometry test alone is not sucient
to make a diagnosis of a clinical condition. Test interpretation and suggested treatment must be pro­vided by a Healthcare professional.
A correct spirometry test depends
on the user’s capability to inhale
and exhale all air completely and as fast as possible. If these fun­damental conditions are not re­spected then the results obtained during spirometry testing will not
be accurate, and therefore the test
results are “not acceptable”.
The acceptability of a test is the responsibility of the user. Special attention should be given when
testing the elderly, disabled and
children.
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The device should never be used when it is possible or probable
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that the validity of the results may be compromised due to any external factors.
Some conditions may pose a relative danger to a patient or
aect 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 dam­age 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
certied the conformity of the device
to the European Safety Standards EN 60601-1 and guarantees the EMC Requirements within the lim­its set in the European Standard
EN 60601-1-2 and ETSI’s
EN 300328. 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 require­ments set by the Council Directive 93/42/EEC for medical devices.
• Use only with iOS and Android
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devices specied on our website
www.nuvoair.com.
• Use only in environments speci-
ed in this user manual.
• Do not expose to liquids.
• Air Next is not made with natural rubber latex.
• Should you lose the battery hatch with required and device
specic 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.
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Explanation of the safety signs and symbols marked on the device:
Manufacturer’s name and address.
CE mark: indicates that the device
is certied that it conforms to the
0598
requirements of the 93/42/EEC medical device directive.
IP classication: 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. Do not dispose as unsorted municipal waste.
Manufacturer’s LOT batch/lot code.
Follow operating instructions: Indicates the need for the user to consult the instructions for important information.
The symbol is used in accordance with IEC 60601-1-2:2014 (ED. 4) for products including radio trans- mitters and in accordance with EN 300 328.
Type BF applied part: Device that has conductive contact or medium to long term contact with the
patient in order to fulll the
intended use.
This device complies with part 15
of the FCC Rules. Operation is subject to the following two conditions: (1) This device may not cause
harmful interference, and (2) this device must accept any interference received,
including interference that may cause undesired operation.
FCC ID Identication showing traceability
to FCC compliance.
Caution: Federal law restricts this device to sale by or on the order of a physician
OPERATING ENVIRONMENT
Air Next has been designed for use
in a doctor’s oce, in a hospital
setting or at home.
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Air Next is not intended for use in an operating theatre nor in the
presence of inammable liquids or detergents, nor in the presence of inammable anaesthetic gases
(oxygen or nitrogen). The device is not designed to be used in direct
air currents (e.g. wind), sources of heat or cold, direct sun rays or other sources of light or energy, dust, sand or any other chemical
substances.
NUVOAIR
DISPOSABLE TURBINE
Air Next is designed to be used with NuvoAir disposable single use turbines. The disposable turbine is indicated for single use single patient only. The integrity and functionality is guaranteed by:
• Never holding the turbine under
a jet of water or air and never let it come into contact with high
temperature uids.
• Not allowing dust or foreign
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bodies to enter the turbine
sensor, in order to avoid incorrect
EN
functioning and possible damage. The presence of any impurities
such as hair, sputum, threads etc.
within the body of the turbine sensor may seriously compromise the accuracy of the measurements.
• Avoiding environmental contamination by cleaning waste
products, the user must adhere
to all relevant regulations.
The single use turbine cannot be used to perform a spirometry test on another individual (person). You can purchase new single use turbines at www.nuvoair.com
CAUTION: RISK OF
CROSSCONTAMINATION
Each new individual that uses Air Next shall use a new unused disposable NuvoAir disposable turbine. If the turbine is not
replaced between individuals there is a high risk of infectious cross contamination.
AIR NEXT TESTS
PARAMETERS SUCH AS:
FEV1 (Forced Expiratory Volume
in 1 second) The volume of air (l)
exhaled in the rst second during a forced maximal expiratory eort
after a full inspiration.
FVC (Forced Vital Capacity) The
total volume of air (l) exhaled dur­ing a forced maximal expiratory
eort after a full inspiration.
FEV1/FVC (Ratio) The calculated
result obtained by dividing FEV1 with FVC.
PEF (Peak Expiratory Flow) The
maximum ow rate (l/s) during a forced maximal expiratory eort
after a full inspiration.
The nal results displayed in the
application are always the best values obtained after performing
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the desired number of tests included in a session. The rec­ommended number of tests per
session is 3, however the user can
perform up to 8 tests.
Displayed test are compared to a reference table (GLI) and displayed as percent predictive value (%pred.).
The reference used in Air Next uses expected normal lung func-
tion values such as for FEV1, FVC, FEV1/FVC and PEF are based on ethnicity, gender, age and height.
Interpretation of spirometry results should be made by a physician or allied health care professional
with sucient training in the
performance and interpretation of spirometry.
Note: Home use of Air Next is in­tended only for indicative purpose. Interpretation of the test results and diagnosis shall be done by a healthcare professional.
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MAINTENANCE
Handle Air Next device carefully. Store it in clean and moisture free
conditions. Before use, always check that the device is free from dust,
contamination or any particles.
Air Next does not require profes-
sional maintenance. If, however,
the outside of the device needs to be cleaned make sure to only use a damp cloth without any detergents. The batteries of Air Next are replaceable.
ACCESS TO BLUETOOTH
Enable Bluetooth on your mobile device in order to pair with the Air Next. You can enable Bluetooth in your mobile device settings. Check your device manual on how to do this.
ELECTROMAGNETIC COMPATABILITY
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EN
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EN
BLUETOOTH PROXIMITY
Make sure that the Air Next is within the Bluetooth proximity of your phone. If your phone is too
far away from the Air Next, the
connecton could be lost.
FCC RADIO FREQUENCY INTER­FERENCE STATEMENT
This equipment has been tested and found to comply with the
limits for a Class B digital device,
pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates uses and can radiate radio frequency energy
and, if not installed and used in accordance with the instructions,
may cause harmful interference to
radio communications. However,
there is no guarantee that interfer­ence will not occur in a particular installation. If this equipment does cause harmful interference to
radio or television reception, which
can be determined by turning the
equipment o and on, the user is
encouraged to try to correct the interference by one or more of the following measures:
· Reorient or relocate the receiving
antenna.
· Increase the separation between
the equipment and receiver.
· Connect the equipment into an outlet on a circuit dierent
from that to which the receiver is connected.
· Consult the dealer or an
experienced radio/TV technician for help.
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NuvoAir is not responsible for any radio or communication interfer­ence caused by using other than
specied or recommended cables
and battery or by unauthorized
changes or modications to this equipment. Changes or modi-
cations not expressly approved by the manufacturer could void
the user’s authority to operate the
equipment. This device complies with part 15 of the FCC Rules. Operation is subject to the following two conditions:
1. This device may not cause
harmful interference, and
2. This device must accept any
interference received, including
interference that may cause unde­sired operation.
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TROUBLESHOOTING
• Make sure that the NuvoAir Disposable Turbine is correctly inserted into Air Next.
• Make sure that the turbine is not spinning before you do a test.
• Make sure that Air Next has
sucient battery levels.
• Make sure that Bluetooth is enabled on your mobile device.
• Make sure the app is allowed to use Bluetooth.
• The device can be aected by its environment if it is too bright. Try dimming the light or move to a darker location.
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TECHNICAL FEATURES
EN
Environment of use All settings
Patient Population Adults and pediatric patients over 5 years old
Technology for measure ow and volume Bidirectional turbine with infrared interruption
Energy Type Two AAA 1.5V Alkaline batteries
Physical Conguration Touchscreen on smartphone or tablet
Operating environment T: min +10°C/max +40° C RH: min 10 %/max 95 %
Conditions of storage T: min -20°C/max +60° C RH: min 10 %/max 95 % P:
Dimensions 98 x 62 x 26 mm
Weight 75g
Volume accuracy ±3% of reading or ±0.050 L, whichever is greater
Volume range 0.5-8L
ALT: max 2000 m
min 500 mBar / max ALT: ≤ 5000 m
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Flow range 0-14L/s
Flow accuracy ±5% or 200 mL/s
Flow resistance <0.5 cmH2O/L/s
Communication Bluetooth
Coaching Display of ow-time curves, timer and eort during test
Life expectancy 10 years
Regulations applicable: MDD 93/42 /EEC
RF emissions CISPR 11 Group 1
RF emissions CISPR 11 Class B
ISO 26782 ISO 23747 Electrical Saftey IEC 60601-1 Electro Magnetic Compability IEC 60601-1-2 EN 300 328
FCC Part 15, Subpart B, C
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EN
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NuvoAir AB
Riddargatan 17D, SE-11457 Stockholm,
Sweden
Version 1.0 © 2018 NuvoAir AB
NuvoAir AB guarantees that the product is free from material and
fabrication defect, under normal
use conditions and under the warranty period.
For more information about the
warranty, for reclamation or to provide feedback, please visit
www.nuvoair.com
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Riddargatan 17D, SE-11457 Stockholm, Sweden
Version 1.0 © 2018 NuvoAir AB
NuvoAir AB
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