Devilbiss Guidance And Manufacturer's Declaration; Guidance And Manufacturer's Declaration; Guidance And Manufacturer's Declaration - Electromagnetic Immunity - DeVilbiss Healthcare iGo 306DS Manual Del Usuario

Pressure Relief Mechanism .......................................................................................................................................................................................... 20 psi ±20% (138 kPa ± 20%)
OSD Set Points ...............................................................................................................................................................................................................≥ 84% - Normal Light (green)
Device Classification .......................................................................................................Class 1, Type BF Applied Part, IPX1 (Battery Mode Only), IPX0 (AC and DC Input Mode)
The DeVilbiss iGo Oxygen Concentrator meets RTCA DO-160F Section 21 Class M for battery operation only Airline Use.
electrical Power:
DeVilbiss Rechargeable Battery (Lithium Ion) ...................................................................................................................................................................................... 8.8 Amp Hrs
AC Adapter Input Voltage Range ......................................................................................................................................................................................... 100-250Vac, 50/60 Hz
DC Adapter ......................................................................................................................................................................................................... 12 Volt Negative Ground Vehicles
Adapter manufacturer Info:
AC Adapter ..............................................................................................................................................Jerome Industries Model # WSX828M, Autec Model # DT-EM250-2805
DC Adapter .........................................................................................................................................................................................................................EDAC, Model ED1010E
Audible Alerts:
• Power Fail
• Low Battery
CAUTION–When moving the iGo from an extreme environment, allow time for your iGo to acclimate to the recommended operating environment. Operating your iGo outside
the recommended operating environment may impact performance, cause damage, and will void the warranty.
Specifications subject to change without notice.
DeVilbiss will make available on request circuit diagrams, parts lists, etc.

deVIlbISS GuIdAnce And MAnuFActurer'S declArAtIon

WArnInG
Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and put into service according to the Electromagnetic
Compatibility [emC] information provided in the accompanying documents.
Portable and Mobile RF Communications Equipment can affect Medical Electrical Equipment.
The equipment or system should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary, the equipment or
system should be observed to verify normal operation in the configuration in which it will be used.
NOTe– TheEMCtablesandotherguidelinesprovideinformationtothecustomeroruserthatisessentialindeterminingthesuitabilityoftheEquipmentorSystemforthe
Electromagnetic Environment of use, and in managing the Electromagnetic Environment of use to permit the Equipment or System to perform its intended use without
disturbing other Equipment and Systems or non-medical electrical equipment.
Guidance and manufacturer's declaration – electromagnetic emissions
This device is intended for use in the electromagnetic environment specified below. The customer or the user of this device should assure that it is used in such an
environment.
emissions Test
RF Emissions CISPR 11
RF Emissions CISPR 11
Harmonic emissions IEC 61000-3-2
Voltage fluctuations / flicker
emissions
Guidance and manufacturer's declaration – electromagnetic Immunity
This device is intended for use in the electromagnetic environment specified below. The customer or the user of this device should assure that it is used in such an environment.
Immunity Test
Electrostatic discharge (ESD)
IEC 61000-4-2
Radiated RF IEC 61000-4-3
Conducted RF IEC 61000-4-6
Electrical fast transient
IEC 61000-4-4
Surge IEC 61000-4-5
Power frequency magnetic field
IEC 61000-4-8
Voltage dips, short interrupts and
voltage variations on power supply
input lines IEC 61000-4-11
en - 12
• Low Oxygen Output
• High Flow/Low Flow
• No Breath Detected in PulseDose Mode
Compliance Electromagnetic Environment – Guidance
This device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not
Group 1
likely to cause any interference in nearby electronic equipment.
Class B
Class B This device
the public low-voltage power supply network that supplies buildings used for domestic purposes.
Complies
IEC 60601 Test Level Compliance Level
±6kV contact
Complies
±8kV air
3 V/m 80MHz to 2.7GHz Complies
3 Vrms 150kHz to 80MHz Complies
±2kV power line
Complies
±1kV I/O lines
±1kV differential
Complies
±2kV common
3 A/m Complies
>95% dip 0.5 cycle
60% dip 5 cycles
Complies
70% dip 25 cycles
95% dip 5 secs.
is suitable for use in all establishments including domestic and those directly connected to
Electromagnetic Environment - Guidance
Floors should be wood, concrete, or ceramic tile. If floors are covered with
synthetic material, the relative humidity should be at least 30%
Field strengths outside the shielded location from fixed RF transmitters, as
determined by an electromagnetic site survey, should be less than 3 V/m.
Interference may occur in the vicinity of equipment marked with the following
symbol:
Mains power quality should be that of a typical commercial or hospital
environment.
Power frequency magnetic fields should be at levels characteristic of a typical
location in a typical commercial or hospital environment.
Mains power quality should be that of a typical commercial or hospital
environment. If the user of this device requires continued operation during
power mains interruptions, it is recommended that the device be powered from
an uninterruptible power supply or battery.
75-85% - Low O
< 75% - Service Required Light (red) and Audible Alert
• High Temperature
• Unit Malfunction
Light (yellow)
2
A-306-1