Atmos E 2 User manual

MedizinTechnik
ATMOS
Patient Chair E 2
535.0000.B
535.0000.B with option:
electrical backrest
2015-01 Index: 04
Patient Chair E 2
Operating Instructions
English

2
Further information, accessories, consumables and
spare parts are available from:
ATMOS
MedizinTechnik GmbH & Co. KG
Ludwig-Kegel-Straße 16
79853 Lenzkirch
Deutschland / Germany
Tel. +49 76 53 689-0
Fax: +49 76 53 689-190
+49 76 53 689-493 (Service Center)
www.atmosmed.de
Contents
1.0 Introduction ............................................................... 3-5
1.1 Notes on operating instructions...................................... 3
1.2 Intended use .................................................................. 3
1.3 Function ......................................................................... 3
1.4 Explanation of pictures and symbols.............................. 4
1.5 Scope of supply.............................................................. 5
1.6 Transport and storage .................................................... 5
2.0 For your safety ............................................................. 6
3.0 Setting up and starting up........................................ 7-8
3.1 Setting up ...................................................................... 7
3.2 Starting up...................................................................... 7
3.2.1 Front view....................................................................... 7
3.3 Power connection........................................................... 8
4.0 Operating ................................................................. 9-12
4.1 Positioning the patient.................................................... 9
4.1 Adjusting the seat height................................................ 9
4.2 Rotating the upper part of the chair.............................. 10
4.3 Rotating the seat .......................................................... 10
4.4 Adjusting the backrest...................................................11
4.5 Back rest movement, electrical .....................................11
4.6 Adjusting the arm rests .................................................11
4.7 Adjusting the head rest ................................................ 12
4.8 Foot rest ...................................................................... 12
4.9 Chassis (optional) ........................................................ 12
5.0 Cleaning ................................................................ 13-14
5.1 General information on cleaning and disinfection ........ 13
5.2 Cleaning the unit's surfaces and up olstery.................. 13
5.3 Recommended surface disinfectants ........................... 14
5.4 Recommended disinfectants for the upholstery^14
6.0 Maintenance and service........................................... 15
7.0 Trouble-shooting........................................................ 15
8.0 Accessories and Spare Parts.................................... 16
8.1 Accessories.................................................................. 16
8.2 Spare parts................................................................... 16
9.0 Technical specifi cations............................................ 17
10.0 Disposal ...................................................................... 18
11.0 Notes on EMC........................................................ 19-21
General tems and conditions

3
1.3 Function
1.0 Introduction
1.1 Notes on operating instructions
These operating instructions contain important notes on how to operate the ATMOS Patient chair
E2 safely, correctly and effectively. Their reading helps to avoid risks, and also to reduce repair
costs and down-time. That increases, amongst other things, the reliability and service-life of the
device.
These operating instructions serve not only for new operating personnel to be instructed in its use,
but also for use as a reference manual.
These operating instructions must always be kept available near the device.
Care and safety inspections in conjunction with professional execution provide for operational safety
and readiness for use of your ATMOS Patient chair E2 and are therefore a must besides regular
cleaning.
Repair work and safety inspections may be carried out only by expert personnel authorised by
ATMOS. By applying only original spare parts you will have the guarantee that operational safety,
readiness for work and the value of your ATMOS Patient chair E2 will be preserved.
● The product ATMOS Patient Chair E 2 bears CE marking CE according to the EC
Directive of the council for medical products 93/42/EEC, Directive 2007/47/EC dd.
05 September 2007 and meets the basic requirements of annex I of this directive.
● The product ATMOS Patient Chair E 2 complies with all applicable requirements of the directive
2011/65/EC restricting the use of certain hazardous substances in electrical and electronic
equipment (“RoHS”).
● The declaration of conformity can be obtained on our website at www.atmosmed.com.
● The quality management system applied at ATMOS has been certi ed according to international
standards EN ISO 9001 and EN ISO 13485.
● Prior to start-up please peruse chapter 2.0 „For your safety“, in order to be prepared for any
possible dangerous situations.
The patient chair has an electromotive height adjustment
from 58,5 cm – 78,5 cm. The height adjustment is controlled
by a foot switch. The Auto - Down (homing) function drives
the chair automatically to its lowest position, if so desired.
The upper part of the chair rotates and can be locked at any
desired position by a hand lever operated locking mecha-
nism. The tall, reclining backrest moves from +7° forward
to fully horizontal. The easy to remove neck support is also
height adjustable. The separately swivelling chair top rotates
90° left or right and features a snap lock for center, left or
right stop.
1.2 Intended use
Name: ATMOS®Chair E 2
Main functions:
This patient's chair enables the optimum positioning of the pa-
tient with regard to height and access.
Med. indications/ application:
Positioning of the patient during standard ENT examinations
and / or therapy.
Specifi cation of the main function:
• Electromotive height adjustment by pedal switch from 58.5 cm
to 78.5 cm
• The upper part of the chair rotates around 360° and is
equipped with an arrestor on both sides;
with an electrical backrest by 300°.
• Seats with integrated handles separately rotary both 90° to
the right and to the left
• In nitely variable inclination of the backrest from +7° forward
to the horizontal position (mechanical or electric)
• Height adjustable and detachable headrest
• Armrests can be folded up (individually)
• Foot support, synchronous coupling with the backrest
Application organ: Positioning of the patient
Application time: Temporary (max. 60 minutes)
Application site: In clinics and practices for ENT doctors and
phoniatrists. The application of the doctor’s chair must be exe-
cuted by medically trained persons only.
Contraindications: None
The product is: X active □ not active
Sterility: Not necessary
Single use product / reprocessing: No single use
product

4
1.4 Explanation of pictures and symbols
1.0 Introduction
!
■
●
→
click
click
Symbols within these operating instructions
Warning,
especial diligent notice!
Short cuts / symbols contained in this manual
Please press where
the dot indicates
Subnumeration
Numeration
General information
Follow the arrows whilst
proceeding, sequence
Checking
Please read,
important information
Important notes
Symbols of the ATMOS patient chair E 2
Order number
The CE sign shows that this product
meets the appropriate requirements
of the EC guidelines.
Application part type B
REF
Exchange
Move, plug ...
in this direction
Engage,
then check correct t
Turn, shift ...
in this direction
Alternating current
~

5
1.0 Introduction
1.5 Scope of supply
●Prior to dispatch, the ATMOS patient chair E2 was subjected to an extensive functional test and has been carefully packed.
Nevertheless, please compare the contents of the shipment on completeness immediately upon receipt (see delivery note).
Basic device
Operating
instructions
1.6 Transport and storage
●The transport of the device may be effected only in a dispatch
carton upholstered and offering suf cient protection.
●Please document and report damages in transit immediately.
For complaints or return deliveries, please use the enclosed
form QD 434.
●The unit must be allowed to stand for up to six hours at room
temperature prior to starting up for the rst time following
transport at temperatures below freezing. The unit may not
be operated if it has not acclimatised as this might damage
the motor.
●Ambient conditions:
Transport/Storage: -10...+50°C;
30...95 % air humidity
non-condensing
at air pressure 500...1060 hPa
Operation: +10...+35°C;
30...95 % air humidity
non-condensing
at air pressure 700...1060 hPa
Mains cable

6
!
For your safety
2.0 For your safety
• The ATMOS patient chair E2 is designed in accordance
with IEC 601/EN 60601. The chair conforms to VDE
protection class I. It may only be connected to a correctly
installed shockproof socket.
• The chair may only be operated under constant supervision
(IEC 601-1/EN 60601-1).
• Prior to starting the chair for the rst time, check whether
the supply voltage indicated on the line voltage selector
corresponds to the value of your local mains supply.
• The power cable supplied with the chair (or an equivalent
one) must be used exclusively for connection to the mains
supply.
• Observe correct wiring when installing plugs speci c to
foreign countries:
green/yellow: ground conductor
blue: neutral conductor
black or brown: phase
• Prior to starting the chair, check whether connecting cables
show signs of damages. Damaged cables must be re-
placed.
• For the purpose of separating the chair from the mains, the
mains plug must always be pulled out of the wall socket rst
before unplugging the power cable from the chair. Never
touch power cord or plugs with wet hands.
• The ambient conditions speci ed in section 7.0 "Technical
speci cations" must be strictly observed.
• The ATMOS patient chair E2 is not intended for operation
in areas of medical rooms subject to danger of explosion.
Areas subject to explosion hazards may be created by the
use of in ammable anaesthetics, skin cleansers and disin-
fectants.
• Ensure that your patients sit in the middle of the seat.
A constant unilateral strain on the seat can damage the
surface.
• The user must be familiar with the operation of the chair.
• ATMOS cannot be held liable for injury to persons or
damage to property if
- the parts used are not original ATMOS parts,
- the user instructions given in this manual are
disregarded.
• Please note:
A medical insulating transformer with earth leakage
monitor or any similar safety system acc. to EN 60 601-1 is
required, if several devices are connected over one common
power supply. The transformer must correspond to the power
consumption of all the devices to be connected.
• The electric motor is protected by an integrated thermo
protection switch. After 1.5 minutes of continued operation,
the motor needs a cool down period of approx. 8.5
minutes. If the thermo protection switch activates, the
motor needs a cool down period of approx. 20 minutes

7
Fig. 1.
3.0 Setting up and starting up
3.1 Setting up
Make sure, product is set up on level, solid oor.
Line power and fuses
Line power : 230V / 50Hz (120V / 60Hz)
Fuses: Thermal fuse: 3 A (230V)
Thermal fuse: 6 A (120V)
3.2 Starting up
● Set up product at desired spot, make sure oor is even
and level.
● Make sure suf cient space is available for proper rotation
of the upper part of the chair.
● Before rst operation of chair, read and observe the safety
instructions in section 2.0.
●Finally, connect power cord.
3.2.1 Front view
Individually adjustable headrest
Lever for in nitely variable synchronous adjustment
of the backrest, arm rests and foot support
Arm rests to be swivelled off backwards
Rotary seat
Lever for arresting the rotary upper part of the chair
Swingable foot support
Foot switch for adjusting the seat height

8
3.3 Power connection
Connect the ATMOS E 2 chair to line power using the included
IEC power cord. Insert the power cord to the IEC socket at
the back side of the chair base and the wall mounted power
outlet.
Make sure, power outlet features a proper ground connection.
Find all relevant electrical data (voltage and nominal frequency)
as well as the data for fuses on the label located over the
socket.
To disconnect the device, pull the power cord out of outlet
socket.
There is no indication, that product is hooked up to
line power.
Disconnect chair, if not in use, during service and
repair work and or for cleaning.
3.0 Installation and start-up

9
4.0 Operating
To adjust the chair height, press the left foot switch for up, and the
right foot switch for down movements.
The arm rests fold away backwards, which will assist incapacitated
people to shift from a wheelchair into the examination chair.
The in nitely adjustable backrest is locked / unlocked by a release
lever on either side of the backrest.
Arm rests, base part and back rest are coupled for synchronous
movements.
The drive unit has an integrated thermo switch. This means that
continous operation of the drive unit is only possible for max. 1.5
min, after this period of time a rest period of approx. 8.5 min is re-
quired. If continuous operation exceeds 1.5 min, the thermo switch
is activated and after that operation is only possible after approx. 20
minutes cooling period.
!
4.2 Adjusting the seat height
Height adjustment of seat cushion level is controlled by 2 foot
switches ( g.2)
= Left foot switch = up
= Right foot switch = down
Furthermore, the ATMOS patient chair features an “Auto –
Down (homing)” function, driving the seat down to its lowest
level after a short tap on the foot switch. Pressing the right
foot switch for less than 0.5 seconds will move the chair
to home position. To stop the movement, just brie y tap the
switch again.
Fig. 2
4.1 Positioning the patient
Ensure that your patients sit in the middle of the seat. A constant
unilateral strain on the seat can damage the surface.

10
Fig. 3
Locking lever
4.3 Rotating the upper part of the chair
The upper part of the chair with the patient can be completely
rotated after having loosened the brake with the locking lever
(, Fig. 3).
The upper part with the patient can then be rotated in the
desired direction.
If the brake is only slightly xed the chair can be rotated without
loosening the brake.
The rotating angle is limited for chairs with an electrical back-
rest adjustment. In this case the chair can be rotated by 150°
either to the right or to the left.
4.4 Rotating the seat
The seat with the patient can be rotated independent of a
backrest movement.
To do so, adjust the lateral locking lever (, Fig. 4) beyond
its central position. The seat can then be rotated 90° to the
left or 90° to the right. If the locking lever (, Fig. 4) is moved
to central position, the seat is slightly xed both in position
90° left and 90° right and snaps in central position.
Fig. 4 Locking lever
4.0 Operating

11
4.0 Operating
Fig. 7 Arm rests
4.7 Adjusting the arm rests
The arm rests (Fig. 7) can be individually swivelled off
backwards.
4.5 Adjusting the backrest
– Press lever element (, Fig. 5) downwards,
– adjust backrest to the desired position,
– release lever element which will then return to
its initial position,
– backrest and foot support are arrested.
Arm rests, foot section and backrest are coupled and change
their positions synchronously.
Fig 5
Lever element
4.6 Back rest movement, electrical
The arm rests, foot rest and back rest are mechanically inter-
locked and move synchronized.
As an option, electric actuators are available to move the back
rest of the ATMOS E 2 patient chair.
The electric back rest movement is controlled by one foot switch
(, Fig. 6) in the base cover and two toggle switches, located
in the side of the back rest.
In the up movement, the back rest will rst stop at the vertical
position. To move the back rest to the + 10° forward lean posi-
tion, press any of the switches again.
Fig. 6 Foot switch

12
4.0 Operating
4.8 Adjusting the head rest
The headrest can be adjusted to a lower position by simply
pulling out the retaining band; a higher position is reached by
pushing the band in. For removing the headrest, pull the retaining
band completely out of the backrest.
Fig. 8 Headrest
4.9 Foot rest
If required, the foot rest can be folded down (Fig. 9).
4.10 Chassis (optional)
Do not transport any weights or persons on the chair.
The chair may be moved as soon as the red light illuminates.
Clearance height: ca. 15mm.
Extend the chassis:
• Move the chair upwards until the green light illumi-
nates (, g 10).
• Push the lever to the left (, g. 12) to extent the
chassis.
• Move the chair downwards until the red light illumi-
nates (, g. 10).
The chair can now be moved.
Retract the chassis:
• Move the chair upwards until the green light illumi-
nates (, g. 10).
• Push the lever forward (, g. 11) to retract the chas-
sis.
• Move the chair to the desired position / .
LEDs ( g. 10)
Red: extend the chassis, chair can be moved
Green: lever can be adjusted
Lever position ( g. 11 + 12):
Only adjust the lever when the green LED is illuminated
otherwise the chair can get damaged.
Forward: retract the chassis
Left: extend the chassis
!
Fig. 9 Foot rest
Fig. 11 Fig. 12
Fig. 10

13
5.1 General information on cleaning and disinfection
5.0 Cleaning
Before cleaning
Medical devices must always offer a maximum in safety and function.
We therefore recommend:
Prior to each application:
if
necessary
5.2 Cleaning the unit's surfaces and upholstery
If liquid has penetrated the unit, it may not be operated again until it has been checked by the authorised customer
service centre.
●The surfaces of the ATMOS Patient chair E 2 are resistant against all the recommended surface disinfectants stated
in chapter 5.3 and 5.4. Nevertheless after any length of time discolourations could possibly develop. Polar solvents
(e.g. acetone or chlorinated hydrocarbons (CCs)) may not be used for cleaning and disinfecting.
Prior to cleaning and surface disinfection, please disconnect the chair from the mains supply.
●The unit itself can be wiped off with a moist (not wet) cloth.
● Substances such as blood need to be removed immediately to prevent stains on the cover material of the uphol-
stery.
!
The described measures to clean and to disinfect
or sterilize do not rule out regulations valid for the
particular company!
In chapter 5.3 and 5.4 all surface and
instrument disintectants are stated which
are suitable for disinfection.
Always observe the concentration speci cations
and instructions by the respective manufacturer
Do NOT use
• disinfectants containing concentrated organic
or anorganic acids or bases, since these may
cause corrosion damages.
• disinfectants containing chloramides, phenol
derivatives or anionic tensides, since these may
cause stress cracks in the plastics used.
Do not use any abrasive cleaning agents. For the upholstery usual dry foam may be used. Treatment with a commonly
used care product for arti cial leather is recommended once a week in order to keep the upholstery soft and smooth.
!

14
5.3 Recommended surface disinfectant
● The surfaces of the ATMOS patient chair E2 can be cleaned/wiped with disinfectants containing the following active
ingredients:
• QAV (quarternary ammonium compounds)
5.4 Recommended disinfectants for the upholstery
Disinfectant Ingredients (in 100 g) Manufacturer
ATMOS Green & Clean SK Alkyldimethylbenzylammoniumchloride < 1 g Metasys, Rum (Austria)
(application solutionungslösung) Dialkyldimehtylammoniumchloride < 1 g
Alkyldimethylethylbenzylammoniumchloride < 1 g
5.0 Cleaning

15
7.0 Trouble-shooting
6.0 Maintenance and Service
The chair does not require any maintenance. However, a blown
out fuse may occur and require replacement (see Chapter
6.1).
In case of malfunctions, please contact your local
authorized ATMOS service technician.
Before commencing this job, make sure to
disconnect the device from line power.
6.1 Fuse exchange
●To open the fuse socket
rotate top counter clockwise
●Exchange of fuse
●To close fuse socket, rotate top cw.
Malfunction Possible cause Solution
Chair does not start up – Mains plug is not connected correctly – Check connection at the socket
– No mains voltage – Check house fuse
– Check mains plug on perfect t at the
device
– Defective fuse – Exchange the fuse
In the case of any malfunction, please immediately inform your authorised ATMOS service.

16
8.0 Accessories and Spare Parts
REF
8.1 Accessories
Child seat on request
8.2 Spare parts

17
9.0 Technical Data
Last update: 09.12.2014
Voltage 230 V~ ± 10 %; 50 Hz
Special voltage:120 V~ ± 10 %; 60 Hz
Current input 2,5 A (ca. 3,1 A with the additional electrical back-rest adjustment)
Power consumption 520 VA (ca. 700 VA with the additional electrical back-rest adjustment)
Fuses 3,15 A T
Operating time max. 1.5 min operation and afterwards 8.5 min rest period
Seat depth length: 490 mm, width 480 mm
Seat height 585 mm up to 785 mm
Vertical lift 200 mm
Vertical speed 13 mm/sec.
Lifting capacity / load 150 kg
Height adjustment 200 mm (double: "lifting")
Rotation 360° without detent
with the option electrical back-rest: 300° (150° right / 150°left) without detent
Height of back rest 900 mm
Back rest inclination + 7 ° bis – 90 ° (horizontal position)
Protective earth conductor resistance
Earth leakage current
Patient leakage current
Enclosure leakage current
—
—
—
n.c. < 0,1 mA
Ambient conditions
Transport/storage
Operation
-10...+50 °C
30...95 % humidity without condensing,
air pressure 500...1060 hPa
+10...+35 °C
30...95 % humidity without condensing,
air pressure 500...1060 hPa
Dimensions HxWxD 1490 mm x 630 mm x 930 mm
Weight 102 kg
with the option electrical back-rest: 104 kg
Weight with the base plate is movable 110 kg
with the option electrical back-rest: 112 kg
Protection class (EN 60601-1) I
Circular safety controls Acc. to accident prevention regulations: every 2 years
Degree of protection Typ B
Protection category IP 20
Classi cation acc. to Annex IX
EC Directive 93/42/EEC
I
CE marking CE
Rules applied EN 60601-1
EN 60601-1-2
UMDNS-Code 10-794
REF 535.0000.0
534.0000.4 (Special voltage)

18
● The ATMOS patient chair E2 does not contain any hazardous materials.
● The housing is recyclable.
● Device and accessories must be decontaminated prior to disposal.
● Please take care on a careful separation of the different materials.
● Please observe national disposal regulations (e.g. waste incineration).
Disposal within the EC
The device described above is a high-quality medical product with a long service life. After its life cycle it must be disposed
of professional. According to the EC directives (WEEE and RoHS) the device may not be disposed of in domestic waste.
Please observe existing national laws and rules for disposal of old devices.
Disposal within the Federal Republic of Germany
In the Federal Republic of Germany the law for electrical devices (ElektroG) rules the disposal of electrical devices. In order
to guarantee a proper disposal of your old device, please either pass on your old device to your specialised dealer or send
it directly to ATMOS MedizinTechnik for a professional disposal.
Before disposal respectively before transport all parts, which came into contact with the patient must be
thoroughly cleaned, disinfected/sterilised. The device surface must be disinfected.
10.0 Disposal

19
11.0 Notes on EMC
11.1 Guidelines and Manufacturer´s Declaration - Emissions
The ATMOS Patient chair E2 is intended for use in the electromagnetic environment speci ed below. The customer
or user of the ATMOS Patient chair E2 should ensure that it is used in such an environment.
Emissions Test Compliance Electromagnetic Environment - Guidance
Harmonics IEC 61000-3-2 Class A The ATMOS Patient chair E1 is suitable for use in
all establishments, including domestic, and those
directly connected to the public low-voltage power
supply network that supplies buildings used for
domestic purposes.
Flicker
IEC 61000-3-3
Inapplicable
11.2 Guidelines and Manufacturer´s Declaration - Electromagnetic Immunity
The ATMOS Patient chair E2 is intended for use in the electromagnetic environment speci ed below. The customer
or user of the ATMOS Patient chair E2 should ensure that it is used in such an environment.
Immunity Test IEC 60601-
Test Level Compliance Level Electromagnetic
Environment - Guidance
ESD
IEC 61000-4-2
± 6 kV Contact
± 8 kV Air
± 6 kV Contact
± 8 kV Air
Floors should be wood, concrete,
or ceramics tile. If oors are
synthetic,
the relative humidity should
be at least 30%.
EFT
IEC 61000-4-4
± 2 kV Mains
± 1 kV I/Os
± 2 kV Mains
± 1 kV I/Os
Mains power quality should be that
of a typical commercial or hospital
environment.
Surges
IEC 61000-4-5
± 1 kV
symmetric
± 2 kV
symmetric
± 1 kV
symmetric
± 2 kV
symmetric
Mains power quality should be that
of a typical commercial or hospital
environment.
Power Frequency
50/60 Hz
Magnetic eld
IEC 61000-4-8
3 A/m Inapplicable
Power frequency magnetic elds
should be that of a typical
commercial or hospital
environment.
■ Medical electrical equipment is subject to special precautions with regard to EMC and must be installed acc.
to following EMC notes.
■ Portable and mobile HF communication facilities can in uence medical electrical equipment.
■ The use of other accessories, other converters and cables than stated may lead to an increased emission
or a reduced interference immunity of the equipment or system.
The device may not be used directly next to other devices or piled up with other devices.
If operation next to or piled with other devices is necessary, please watch the device to check its intended
operation in this arrangement.

20
11.0 Notes on EMC
Immunity Test IEC 60601-
Test Level
Compliance Level Electromagnetic
Environment - Guidance
Voltage Dips / Dropout
IEC 61000-4-11
< 5 % UT
(> 95 % Dip of the UT)
for 0.5 Cycle
40 % UT
(60% Dip of the UT)
for 5 Cycles
70% UT
(30 % Dip of the UT)
for 25 Cycles
< 5 % UT
(>95 % Dip of the UT)
for 5 s
< 5 % UT
(> 95 % Dip of the UT)
for 0.5 Cycle
40 % UT
(60% Dip of the UT)
for 5 Cycles
70% UT
(30 % Dip of the UT)
for 25 Cycles
< 5 % UT
(>95 % Dip of the UT)
for 5 s
Mains power quality should be that
of a typical commercial or hospital
environment. If the user of the
ATMOS Patient chair E2 demands
continued function even in case of
interruptions of the energy supply,
it is recommended to supply the
ATMOS Patient chair E2 from an
uninterruptible current supply or a
battery.
NOTE UTis the mains alternating current prior to application of the test levels.
11.3 Guidelines and Manufacturer´s Declaration - Immunity
The ATMOS Patient chair E2 is intended for use in the electromagnetic environment specied below. The customer or
user of the ATMOS Patient chair E2 should ensure that it is used in such an environment.
Immunity Test IEC 60601-
Test Level Compliance Level Electromagnetic Environment
- Guidance
Conducted RF
IEC 61000-4-6
3 Veff
150 kHz up to 80
MHz
3 V
Portable and mobile communications
equipment should be separated from the
Patient chair E2 incl. the cables by no less
than the distances calculated/listed below.
Recommended distances:
d = 3,5/3 √ P
d = 3,5/10 √ P
d = 7/10 √ P
where „P“ is the max. power in watts (W)
and D is the recommended separation
distance in meters (m).
Field strengths from xed transmitters, as
determined by an electromagnetic site (a)
survey, should be less than the compli-
ance level (b).
Interference may occur in the vicinity of
equipment containing following symbol
Radiated RF
IEC 61000-4-3
3 V/m
80 MHz up to 2,5
GHz
10 V/m
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