PARAMOUNT BED PA-90000 Series User manual

7A10625900A4
PARAMOUNT BED CO, LTD.
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INSTRUCTION MANUAL
PA-90000 Series Bed
Preface
The correct operang procedures should be explained not only to
the persons using the bed but also to caregivers.
Aer reading this instrucon manual, store it where it can be easily
accessed for later reference.
Users and/or carers are requested to report informaon about any serious
incident related to this bed that occurs within the EU to the manufacturer
and the regulang authority of the member country of residence.‘Serious
incident’ means any incident that directly or indirectly led, might have led
or might lead to any of the following:
a) The death of a user, carer or other person.
b) The temporary or permanent serious deterioraon of a user’s, carer’s or
other person’s state of health.
c) A serious public health threat.
The actual product purchased may differ from detailed descripons
given in this instrucon manual due to product improvements.
Value in the specificaon such as working range, dimensions, angles
and mass are subject to normal manufacturing tolerances. Besides some
exempons, display purpose words such as “approximately”, “about”
etc. are omied.
For any queries, please feel free to contact your dealer directly.
Before using this bed, please read this instrucon manual to fully
understand the safe and proper operang procedures.
Thank you for purchasing the PA-90000 Series Bed.
This instrucon manual describes precauons and how to safely use
and operate the bed.
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CONTENTS
1INTENDED USE / PART NAMES
CONNECTING TO THE POWER SUPPLY (ELECTRIC HOSPITAL BED ONLY)
OPERATION OVERVIEW
USING THE HANDHELD CONTROLLER (ELECTRIC HOSPITAL BED ONLY)
OPERATION PROCEDURES
ASSEMBLING THE BED (PA-90000)
TROUBLESHOOTING
REGULAR INSPECTION AND DAILY MAINTENANCE
2
3
6
Page
1
7
OPTIONAL ACCESSORIES
8
10
11
LONG-TERM STORAGE
MATTRESS (OPTIONAL)
10
SAFETY PRECAUTIONS
SPECIFICATIONS
INSTALLING THE BED
4
5
12
13
14
15
16
1
AFTER-SALES SERVICE
2. IV pole
4-12
13-16
21
22
22
26-27
28
30
31
32
33
38
40
41-43
44-45
46
47
17
24
24
25
29
34
35-36
PRODUCT SYMBOL DEFINITIONS
39
18
4. Oxygen cylinder holder 37
3. Baery (Electric hospital bed only)
BED SIDE TABLE
OVER BED TABLE
19
1. Recommended accessories table
9
1. Aaching/detaching the head board and foot board
2. Aaching the maress stopper
1. Fing component for assembly
1. Power outlet
2. Using the cable storage hooks
1. Handle operaon (Manual hospital bed only)
2. Adjusng the angle of leg secon base
3. Locking the casters
4. Emergency CPR (Back-lowering) funcon (Electric hospital bed only)
2-3
23
ASSEMBLING THE BED (PA-90000VIP)
2. Head board, foot board, side panel installaon 23

INTENDED USE / PART NAMES
1. INTENDED USE

2. PART NAMES
The page number shown next to this
symbol indicates where the related
2
1
Handheld Controller
Head Board
Cable Storage Hooks
Caster
Caster Switching Pedal
Bed with The Central Locking System
Bed with Caster with a stopper
(When the foot board is off)
3-Crank Manual Hospital Bed
(When the foot board is off)
Main Frame
Foot Board
Handle
Caster With Stopper
Power Cable
p.26-27
p.22
p.24
p.22
p.29
p.30
p.28
p.22
p.30
(Applied part)
Part of ME EQUIPMENT that in
normal use necessarily comes
into physical contact with the
※Please refer to the「SPECIFICATION] for the paent target groups and the intended users.
【PA-90000】


The page number shown next to this
symbol indicates where the related
3
p.23
【PA-90000VIP】
Head board
Handheld controller
Leg secon base
Side panel
Caster
Matress stopper
Foot board
Hip secon base
Knee secon base
Power plug
Back secon base
p.26-27
p.29
p.22
Caster switching pedal
p.30
p.23
p.23

Be sure to read these safety precauons beforehand to ensure proper usage.
The safety precauons described here are intended to ensure safe use of the product and prevent
personal injury.
Precauons are classified as “WARNING”, “CAUTION” to indicate the degree of hazard or injury that may
result from improper use. Both are important safety precauons that must be strictly observed. Details
of the pictograms used are shown below. Be sure to fully understand these precauons before reading
the instrucon manual.
Indicates acons that may result in death or serious injury
(broken bones, pressure or paralysis) if the indicaon is ignored.
WARNING
CAUTION
Indicates acons that may result in light personal injury (bruises,
wounds, or cuts) or property damage if the indicaon is ignored.
※Aer reading this instrucon manual, store it in a place that can be easily accessed for later reference.
22 SAFETY PRECAUTIONS
4
[Example pictograms]
This symbol indicates warning or cauonary details. Specifics details are
indicated inside the symbol. (The symbol on the le indicates “Cauon: Electric
shock.”
This symbol indicates acons that are prohibited. Specific setails are indicated
inside or below the symbol. (The symbol on the le indicates “Do not
disassemble.”)
This symbol indicates instrucons or acons that are mandatory. Specific details
are indicated inside the symbol. (The symbol on the le indicates “Unplug
the power plug.”)
[Safety label]
Precauons requiring special aenon by persons
using the bed are affixed to the foot-end frame.
Do not remove or dedace the label.
If the safety label is removed or defaced, replace
with a new one obtained from your dealer.
Electric shock
Do not dissasemble

WARNING
2
5
2SAFETY PRECAUTIONS
Do not put any body part (especially the head or neck) between a fold-down side rail or board and the
raised base ( ).
Even when side rails are used, pay aenon to prevent paents from falling of the bed
A paent may fall off the bed through the gap between a board and fold-down side rail and get
injured.
If a paent bends forward over a fold-down side rail, they may fall off the bed and get injured.
Do not extend the head, hands, or feet outside of the bed.
Do not put any body part (especially the head or neck) between a fold-down side rails and the base or maress.
When the head or neck enters the gap, the paent might not be able to withdraw, and there is a risk
of injury.
A hand or finger may get caught in the gap, resulng in an injury.
Do not insert a head (fingers) and between the bed’s frame and secon base during powered operaon.
Lock the casters at all mes except when moving the bed.
When the head or neck enters the gap, the paent
and/or user might not able to withdraw, and there is a
risk of injury.
Due aenon should be paid to paents who cannot
maintain posture by themselves.
If the bed is operated with a body part (especially
head or neck) placed in the gap, the part may get
caught and injured
The body part may get caught between the lowered
base and the bed’s frame or board and get injured.
The paent may be injured geng on or off the bed
should it move.
Unlock the casters when moving the bed.
Before a paent gets on or off the bed, push down the safety stoppers of the side rail and completely
fold down the side rail.
The paent leg’s could be caught by the side rail, causing
the paent to fall off the bed or the paent’s fingers
could be caught between the supporve bars, causing
injury.
The tubes could be squashed.
Releasing the hands in the middle of the operaon or
slamming the rail down could cause injury or damage
to side rail.
When using IV hanger rod, pay aenon to prevent tubes from geng caught by the side rail.
When folding the side rails, proceed slowly.

WARNING
SAFETY PRECAUTIONS
2
Do not use with infants.
They may fall down through the space of a fold-down
side rail.
Do not allow dust to accumulate on the power plug.
When dust adheres to the surface of the power plug,
the moisture it holds will allow a current to flow, there
will be a worsening of the insulaon condion, and a
risk of fire.
Wipe away any dust accumulang on the power plug
pins and mang surfaces using a dry cloth.
Do not damage cables (including the power cable).
Damage to cables may cause electric shock or a fire.
Prevent cables from geng caught by the bed’s
movable parts.
Do not put heavy objects on cables or apply strong
force
Do not place the bed on cables.
Request repair (or replacement) for damaged cables.
Do not trip over the power cable or cables of the handheld controller.
Damaged plug or cable may induce electric leakage, and in turn, electric shock.
There is a risk of falling down and geng injured.
Do not run cables (including the power cable) of the bed or other electric appliances under the bed.
The cables may get caught in a caster or movable part and damaged, causing a fire or electric shock.
When adjusng the base angle or the bed height, pay aenon to the paent’s condions.
If a paent on the bed moves when adjusng the base angle, they may fall from the bed and get
injured.
Perform the adjusment while supporng the paent who cannot maintain posture by themselves.
If you cannot watch the paent, flaen the base angle and lower the bed to the lowest posion.
If not, the paent may fall off the bed or get caught in a space of a fold-down side rail or board and
get injured.
6
Electric shock

WARNING
Do not allow operaon of the bed by a child aged 12 or under, or someone deemed incapable of
comprehending the operaon.
When transporng a paent, aach the fold-down side rails.
Do not perform an angle adjusment when the paent is lying face down.
Do not stand up on the bed.
Do not go under the bed or put your head, hand, or foot under the bed.
7
When a child aged 12 or under, or somenone deemed incapable of comprehending the operaon
(such as someone having a cognive illness) operates the handheld controller by themselves, there
is a risk of unexpected injury such as the body becoming caught in the bed by mistake.
If there is a risk of such person touching the handheld controller, disconnect the power plug in order
to prevent an accident caused by incorrect operaon.
When a child aged 12 or under, or someone deemed incapable of comprehending the operaton
(such as someone having a cognive illness) operates the handheld controller by themselves, there
is a risk of unexpected injury caused by geng caught in the bed by mistake. (3-crank gatch bed
only)
There is a risk that the paent could fall from the bed and become injured.
Do not move the bed with holding the fold-down side rails. The side rails may get damaged or
deformed.
Use the bed in the proper orientaon.
Lying down on the bed with incorrect orientaon of
head end and foot end will result in an unnatural
posture when the bed posion is adjusted and this
may cause injury.
Bending the joints in the wrong direcon may result
in injury.
There is a risk of injury due to falling or toppling from
the bed.
You may get caught between the bed’s movable part
and the frame or fold-down side rail, resulng in
injury. Prior to operang the bed, make sure that
there is no obstacles around the bed.

WARNING
SAFETY PRECAUTIONS
2
Do not insert the power plug with wet hands.
8
There is a risk of electric shock due to short-circuing.
Do not spill liquids on the bed.
Do not spill liquids on the bed’s electrical components, such as the motors, handheld controller, or
nurse control panel, otherwise, there is a risk of malfuncon. If liquids are accidentally spilt, unplug
the power plug from the power outlet and contact your dealer.
Do not use a mobile phone or other wireless device in the vicinity of the bed.
This may cause a malfuncon of the bed.
Repair or modificaon is not to be performed by the customer.
There is a risk of abnormal operaon and resulng
injury.
Always unplug the power plug when using electronic medical equipment.
Do not aach a restraint belt to the main frame or side rails.
Operaon in posion such as with the back raised or the knee raised may squeeze the body and
cause injury.
Use the bed properly according to the paent’s medical condion.
Improper use of the bed may adversely affect the paent’s medical condion.
Before the paent or a family member operates the bed, make sure that the doctor or nurses explain
related details given in the instrucon manual and proper usage to suit the paent’s medical
condion.
When leaving the bed, lower the bed to the minimum height.
If a doctor, nurse, or aendant leaves the bed, lower the bed as much as possible according to the
paent’s condions because there is a slight chance that the paent may fall off the bed.
Using electronic equipment (e.g. microwave or
high-frequency medical equipment) at the same me
may cause the bed to malfuncon.
When the bed will be used in conjucon with other
medical equipment, check the safety consideraons
before use.
Electric shock
Do not dissasemble
Unplug

9
the wall, beam, or power outlet on the wall.
CAUTION
When using the bed, make sure that the beds does
not hit the wall beam, or power plug during the
Make sure that there is at least 20 cm clearances
from the wall or beam.
bed could be damaged or deformed and result in
injury.
bed could be damaged or deformed and result in
injury.
The bed should not be used by two or more persons.
This bed is designed for use by one person.
be damaged and result in an injury.
The maximum weight the bed can bear is 204 kg
If a doctor or nurse needs to get on the bed for a
beforehand.
The load to be applied to the bed is less than the
to have the bed periodically inspected
Secure at least 20cm clearance

CAUTION
SAFETY PRECAUTIONS
2
Keep away from heaters.
10
Do not use heaters near the bed. Otherwise, the bed
may be damaged or deformed, or even catch fire.
around the bed, or could cause the bed to be
damage or deformed.
Be sure to use the stopper for the headboard and footboard.
If the board is not mounted properly, the board may
suddenly come off when a staff pushes (pulls) the
boar
If the adjusment is done only by one person, their
hand ma
When moving the bed, watch your step.
Avoid moving over uneven floors.
It may result in a damaged or deformed bed or failure.
If it is necessary, move the bed as slowly as possible.
caught.
There is a risk of injury as a result of being caught
b
You may hit your leg againts the caster switching
Lock
Free
to support their body, resulng in an injury. (see p.19)
and main frame, resulng in injury. (see p.26)

CAUTION
SAFETY PRECAUTIONS
2
Hold the power plug body when unplugging.
11
When holding onto only the power cable and pulling
it to disconnect the plug from outlet, the cable could
be damaged and there is a risk of electrical shock.
Always unplug the bed before cleaning.
electrical shock due to a short circuit.
Do not damage the handheld controller.
short circuit.
When the handheld controller is damaged, request
a repair (or replacement).
gaps, cause interference between products, or lower the product safety which may lead to an injury
or bed failure.
Electric shock

CAUTION
SAFETY PRECAUTIONS
2
Do not spray a spray pe of inseccide directly on the bed.
12
Otherwise, there is a risk that the solvents contained in the inseccide could damage, discolor, or
dissolve the bed casters or other resin parts. Pay due aenon to this; othewise, there is a risk of
unexpected injury due to damaged or dissolved parts.
Inspect the bed regularly.
Depending on the frequency of use and the environment, the product will exhibit wear and
deterioraon. Regularly inspect for parts looseness, the operaon of movable parts, and the
precense of damage.
Beds damage in accidents must be inspected and repair bed before reuse.
Beds damaged in earthquakes, fires, or floods, must be inspected and repaired by your dealer.
Damaged electrically-operated bed may cause electric shock or fire due to a short circuit of
electrical parts or an injury due to abnormal operaon induced by deformaon.

SPECIFICATIONS
13
3
Product Name
Family Name
PA-90000 Series
Model No. (*1)
PA-93485 PA-93385 PA-93275 PA-93175 PA-93295 PA-93195
3 Motors
Auto Contour
Back Raising
Knee Raising
Height Adjusment
Procedure
Electric Hospital Bed
Power Supply Voltage/ Frequency
Motorized
Motorized
Motorized
Motorized
AC 100-240V + 10%V / 50/60Hz
Dimensions
Total Length
Total Width
Total Height
Casters
Power Cable Length
2,158mm
1,040mm 960mm 1,040mm 960mm 1,040mm 960mm
910mm 830mm 910mm 830mm 910mm 830mm
125mm dia.
Double-wheel caster
(Central locking system)
125mm dia.
Single-wheel caster
(Central locking system)
125mm dia.
Single-wheel caster
(Diagonal locking system)
Product Weight 122 Kg 110 Kg 117 Kg 105 Kg 111 Kg 99 Kg
Material
Head/Foot Boards
Base
Main Frame
Safe Working Load (*3)
Height Adjusment Range
Temperature
Humidity
Back-Raising
Height Adjustment
Knee-Raising
Power
PP resin mold items
204 Kgf (2000N)
380mm (with no increments)
5to 400 C
20 to 90%RH
Actuator Type
170VA max.
170VA max.
220VA max.
*3) Safe working load: Maximum load with which the bed can be operated. (The total load of user’s weight and
Service life 8 years (based on Paramount Bed data), excluding consumable items such
as caster
Linear actuator (DC motor)
688[+20, -10] to 1,068 [+20,-10]mm
290[+20, -10] to 670 [+20,-10]mm
741[+20, -10] to 1,121 [+20,-10]mm
343[+20, -10] to 723 [+20,-10]mm
00to 700[+7]0(with no increments)
00to 250[+2.5]0(with no increments)
Duty cycle
duty cycle (2min).

SPECIFICATIONS
14
3
Product Name
Family Name
PA-90000 Series
Model No. (*1)
PA-99285 PA-99185 PA-99275 PA-99175 PA-99295 PA-99195
Back Raising
Knee Raising
Height Adjusment
Procedure
Manual Hospital Bed
Manual
Dimensions
Total Length
Total Width
Total Height
Casters
2,158mm
1,040mm 960mm 1,040mm 960mm 1,040mm 960mm
910mm 830mm 910mm 830mm 910mm 830mm
125mm dia.
Double-wheel caster
(Central locking system)
125mm dia.
Single-wheel caster
(Central locking system)
125mm dia.
Single-wheel caster
(Diagonal locking system)
Product Weight 117 Kg 105 Kg 117 Kg 105 Kg 111 Kg 99 Kg
Material
Head/Foot Boards
Base
Main Frame
Height Adjusment Range
Temperature
Humidity
PP resin mold items
204 Kgf (2000N)
380mm (with no increments)
5to 400 C
20 to 90%RH
Manual
Manual
Service life 8 years (based on Paramount Bed data), excluding consumable items such
as caster
*3) Safe working load: Maximum load with which the bed can be operated. (The total load of user’s weight and
Safe Working Load (*3)
728[+20, -10] to 1,108 [+20,-10]mm
330[+20, -10] to 710 [+20,-10]mm
741[+20, -10] to 1,121 [+20,-10]mm
343[+20, -10] to 723 [+20,-10]mm
00to 750[+7.5]0(with no increments)
00to 450[+4.5]0(with no increments)

SPECIFICATIONS
15
3
Product Name
Family Name
PA-90000 Series
Model No.
PA-93485V
3 Motors
Auto Contour
Back Raising
Knee Raising
Height Adjusment
Procedure
Electric Hospital Bed
Power Supply Voltage/ Frequency
Motorized
Motorized
Motorized
Motorized
AC 100-240V + 10%V / 50/60Hz
Dimensions
Total Length
Total Width
Total Height
Casters
Power Cable Length
2,134mm
1,160mm
910mm
125mm dia. Double-wheel caster (Central locking system)
Product Weight 145 Kg
Material
Head/Foot Boards
Base
Main Frame
Safe Working Load (*2)
Height Adjusment Range
Temperature
Humidity
Back-Raising
Height Adjustment
Knee-Raising
Power
Wood
204 Kgf (2000N)
380mm (with no increments)
5
to 400 C
20 to 90%RH
Actuator Type
170VA max.
170VA max.
220VA max.
*2) Safe working load: Maximum load with which the bed can be operated. (The total load of user’s weight and
Service life 8 years (based on Paramount Bed data), excluding consumable items such
as caster
Linear actuator (DC motor)
Maress Base Height (*1)
Side panel Wood
Duty cycle 2min. (stop me: 18min (*3))
761[+20, -10] to 1,141 [+20,-10]mm
290[+20, -10] to 670 [+20,-10]mm
00to 750[+7.5]0(with no increments)
00to 450[+4.5]0(with no increments)
*1) The maress base height indicates the height from the floor to the maress base surface.
*3)
2000mm
duty cycle (2min).

SAFETY PRECAUTIONS
2
16
3SPECIFICATIONS
Range
When transported or stored When in use
Temperature
Humidity
Air pressure
-10 to 500C 5 to 400C
20 to 90%RH 20 to 90%RH
700 to 1,060hPa 700 to 1,060hPa
: IEC 60601-1:2005+CORR. 1:2006+CORR. 2:2007+
13 years of age or older
*Do not use the bed for children (aged 12 or under) or paent
weighing more than 138kg
Supported age range
Paent
target
groups
※
●
Equipment not suitable for use in the presence of a flammable anaesthec mixture.
: Class 1
Back-raising, knee-raising, height adjustment, side rail raising and lowering operaon.
●Frequently used funcons
Essenal performance
Funcon to support the body of paent, Emergency CPR (back lower) funcon.
●Classificaon and Standards
The electrical hospital bed is designed and manufactured according to the following equipment
classificaon and standards.
Classificaon as medical device in Europe
・
Safety standards applied
・
AM1:2012
: IEC60601-1-2:2014
: IEC60601-2-52:2009 (First Edion) for use with IEC
60601-1:2005 (Third Edion)
: EN 60601-1:2006+A12:2014
: EN 60601-1-2:2015
: EN 60601-2-52:2010
Electric shock protecon
: Class 1, Type B
User weight (min-max) 40kg to 138kg
Minimum user height 146cm
Minimum user body
mass index (BMI) 17
Health care workers, paents, relave of paent, and
maintenance staff
Clinical benefit Paent comfort
Quality paent care and efficient care provision
Intended users

SAFETY PRECAUTIONS
17
For the PA-90000 series, special aenon is required to EMC-related safety.
Install, operate and use bed in accordance with the following informaon.
Bed is intended for use in the electromagnec environment specified by “electromagnec disturbance” of bed.
The following abnormality may occur if using bed in unintended environment.
*The funcon for supporng paent’s weight does not maintain.
●If using the other specified accessories, transducers and cable as a replacement part for internal
components, except for transducers and cables sold by the manufacturer of bed, there is a risk of
increasing the emissions or reducing the immunity of bed.
Use portable RF transciever more than 30 cm away from any part of bed (including peripheral
equipment such as antenna cable and external antenna). If it is used within 30 cm, the bed performance
may degrade.
Bed cannot be used with adjacent to or stacked with other equipment. If it must be used adjacent to or
stacked with other equipment, make sure to monitor that it can operate properly in the locaon where
bed is used.
●
●
Bed is intended for use in clinic, restricted medical facilies, hospital (except near high-frequency surgical instrument,
RF shielded room for magnec resonance). Users or customers must use bed in this environment.
Bed is device that suitable to used in hospital due to emission characteriscs. If it used in housing environment, the
equipment may not provide adequate protecon againts wireless radio frequency transciever. The user may need to take
migaon measures such as relocang or redirecng the device.
No. Cable
1AC power cable
2Handheld controller cable
Maximum length [m] Remarks
4.6
2.2
Without shield
Without shield
Guidance and Manufacturer's Declaraon - Electromagnec Emissions
The PA-90000 Series is intended for use in the following electromagnec environment. The customer or user
ofthe PA-90000 Series should make sure it is used in such an environment.
Emission test Compliance Electromagnec Environment - Guidance
RF emissions
CISPR 11/EN 55011 Group 1
The PA-90000 Series uses RF energy only for its
internal funcons. Therefore, its RF emissions are
low and are not likely to cause any interference
with nearby electronic equipment.
RF emissions
CISPR 11/EN 55011 Class A
Harmonic emissions
IEC 61000-3-2/EN 61000-3-2 Class A
Voltage fluctuaons/
flicker emissions
IEC 61000-3-3/EN 61000-3-3
Complies
The PA-90000 Series is suitable for use in all
establishments other than domesc and those
directly connected to the public low-voltage
power supply network that supplies buildings
used for domesc purposes.

SAFETY PRECAUTIONS
18
Voltage Dips
IEC 61000-4-11
/EN 61000-4-11
Surge
IEC 61000-4-5
/EN 61000-4-5
Electrical
fast transient/burst
IEC 61000-4-4
/EN 61000-4-4
Guidance and Manufacturer's Declaraon - Electromagnec Immunity
The PA-90000 Series is intended for use within healthcare facility environment. Users or customers must use bed
in this environment
Stac electricity
discharge (ESD)
IEC 61000-4-2
/EN 61000-4-2
Immunity test Compliance level
IEC 60601-1-2/EN 60601-1-2
Test level
Power Frequency
Magnec Fields
IEC 61000-4-8
/EN 61000-4-8
Short interupons
IEC 61000-4-11
/EN 61000-4-11
Contact discharge: +8kV
Air discharge: +2kV, +4kV, +8kV, +15kV
Contact discharge: +8kV
Air discharge: +2kV, +4kV, +8kV, +15kV
+2kV Power supply line +2kV Power supply line
Line - line: +0.5kV, +1.0kV
Line - ground: +0.5kV, +1.0kV, +2.0kV
Line - line: +0.5kV, +1.0kV
Line - ground: +0.5kV, +1.0kV, +2.0kV
30 A/m 30 A/m
0% UT: 0.5 cycles
Phase: 00, 450, 900, 1350, 1800, 2250,
2700, 3150
0% UT: 0.5 cycles
Phase: 00, 450, 900, 1350, 1800, 2250,
2700, 3150
0% UT: 1 cycle
70% UT: 25/30 cycles
Single phase: 00
0% UT: 1 cycle
70% UT: 25/30 cycles
Single phase: 00
0% UT: 250/300 cycles 0% UT: 250/300 cycles
Note: UT is the AC Power voltage before applying in the test level

SAFETY PRECAUTIONS
19
Enclosure port
to RF wireless
communicaons
equipment
IEC 61000-4-3
/EN 61000-4-3
Guidance and Manufacturer's Declaraon - Electromagnec Immunity
Immunity test
The PA-90000 Series is intended for use in an electromagnec environment that used wireless RF transciever.
Electrromagnec interference can be prevented by maintaining the minimum distance between RF transciever
and PA-90000 Series depend on the maximum output and frequency of the communicaon device as
recommended below.
IEC 60601-1-2
/EN 60601-1-2
Test level
Compliance
level
(V/m)
Band
(MHz) Service Modulaon
Maximum
power
(W)
Distance
(m)
27V/m
385MHz 27 380-390 TETRA 400
Pulse
modulaon
18Hz
1.8 0.3
28V/m
450MHz 28 430-470 GMRS 460,
FRS 460
FM+5 kHz
deviaon
1 kHz sine
20.3
9V/m
710MHz
9V/m
745MHz
9V/m
780MHz
28V/m
810MHz
28V/m
870MHz
28V/m
930MHz
28V/m
1720MHz
28V/m
1845MHz
28V/m
1970MHz
9
28
28
704-787
800-960
LTE Band 13,
17
Pulse
modulaon
217Hz
0.2 0.3
20.3
20.3
Pulse
modulaon
18Hz
Pulse
modulaon
217Hz
1700-1990
GSM 800/900,
TETRA 800,
iDen 820,
CDMA 850
LTE Band 5
GSM 1800;
CDMA 1900;
GSM 1900;
DECT;
LTE Band 1,3,
4,25;
UMTS
Bluetooth,
WLAN,
802.11 b/g/n
RFID 2450,
LTE band 7
Pulse
modulaon
18Hz
20.3
2400-257028
28V/m
2450MHz
9V/m
5240MHz
9V/m
5500MHz
9V/m
5785MHz
95100-5800 WLAN 802.11
a/n
Pulse
modulaon
217Hz
0.2 0.3