User's Manual

FCC Statement
Note: 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 off and on, the user is
encouraged to try to correct the interference by one of
the following measures:
1. Reorient or relocate the receiving antenna.
2. Increase the separation between the equipment and
receiver.
3. Connect the equipment into an outlet on a circuit
different from that to which the receiver is
connected.
4. Consult the dealer or an experienced adio/TV
technician for help.
5. FCC Caution: To assure continued compliance,
(example – use only shielded interface cables when
connecting to computer or peripheral devices). Any
changes or modifications not expressly approved by
the party responsible for compliance could void the
user’s authority to operate this equipment.
6. 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.
7. This device complies with FCC radiation exposure
limits set forth for an uncontrolled environment. End
users must follow the specific operating instructions
for satisfying RF exposure compliance. This
transmitter must not be colocated or operating in
conjunction with any other antenna or transmitter.
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EMC Tables
AViTA BPM18R is intended for use in the electromagnetic environment
specified below.
The customer or the user of AViTA BPM18R must
make sure that it is used in such an environment.
Guidance and manufacturer’s declaration - Electromagnetic emissions
Phenomenon
Professional healthcare
facility environment a)
HOME HEALTHCARE
ENVIRONMENT a)
Conducted and
radiated RF
EMISSIONS
a) CISPR 11
Group 1 Class B
Harmonic
distortion
Not applicable
Voltage
fluctuations and
flickering
Not applicable
a) The equipment is suitable for use in Home Health Environments and
Professional Health Care Environments limited to patient rooms and
respiratory treatment facilities in hospital or clinics. The more restrictive
acceptance limits of Group 1 Class B (CISPR 11) have been considered and
applied. The equipment is suitable for use in the mentioned environments
when directly connected to the Public Mains Network.
b) The test is not applicable in this environment unless the ME EQUIPMENT
and ME SYSTEM used will be connected to the PUBLIC MAINS NETWORK
and the power input is otherwise within the scope of the Basic EMC
standard.
Guidance and manufacturer’s declaration - Electromagnetic immunity -
Enclosure port
Immunity test levels Phenomenon Basic EMC
standard or test
method
Professional
healthcare
facility
environment
HOME HEALTHCARE
ENVIRONMENT
ELECTROSTATIC
DISCHARGE
IEC 61000-4-2 ± 8kV contact
± 2 kV, ±4kV ±, ±8 kV, ±15 kV air
Radiated RF EM
fields
IEC 61000-4-3 a) 10 V/m b) 80MHz - 2.7
GHz 80% AM at 1kHz
Proximity fields
from RF wireless
communications
equipment
IEC 61000-4-3 COMPLIANT
NOTE: Further information about
distances to be maintained between
portable and mobile RF
communications equipment
(transmitters) and the AViTA BPM18R
can be requested from AViTA using the
contact information provided in this
manual. However, it is advisable to
keep the electromechanical aerosol
equipment at an adequate distance of,
at least, 0.5 m from mobile phones or
other RF communications transmitters
to minimise possible interference.
RATED power
frequency
magnetic fields.
IEC 61000-4-8 30 A/m c)
50 Hz or 60 Hz
a) The equipment is suitable for use in Home Health Environments and
Professional Health Care Environments limited to patient rooms and
respiratory treatment facilities in hospital or clinics. The more restrictive
IMMUNITY acceptance limits have been considered and applied.
b) Before modulation is applied.
c) This test level assumes a minimum distance of at least 15 cm between
the ME EQUIPMENT or ME SYSTEM and sources of power frequency
magnetic fields.
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