AOpen DT2462M Manuel utilisateur

MEDICAL GRADE TOUCH DISPLAY

User Guide

23.8” LCD Touch Screen Monitor

Model: DT2462M

2 / 47

Table of Contents

User Guide

.............................................................................................................................................. 1

1. Introduction ..................................................................................................................................... 3

1.1

Monitor description ............................................................................................................. 3

1.2

Box of contents .................................................................................................................... 3

1.3

Product overview ................................................................................................................ 4

2. Important Information ..................................................................................................................... 8

2.1

Safety information .............................................................................................................. 8

2.2

Environmental information ................................................................................................ 10

2.3

Regulatory information ...................................................................................................... 11

2.4

Equipment Symbols .......................................................................................................... 12

3. Cleaning the Display ....................................................................................................................... 14

3.1

Cleaning instructions .......................................................................................................... 14

3.2

EMC notice ........................................................................................................................ 15

4. Monitor Installation ....................................................................................................................... 22

4.1

Installation procedure ........................................................................................................ 22

4.2

Stand removal & VESA mount installation ......................................................................... 23

5. Daily Operation .............................................................................................................................. 26

5.1

Main power switch ........................................................................................................... 26

5.2

Power/Status indication ..................................................................................................... 26

6. OSD Menu Operation ..................................................................................................................... 27

6.1

On-Screen Display .............................................................................................................. 27

6.2

Menu Descriptions ............................................................................................................. 27

6.3

OSD Structure..................................................................................................................... 27

6.4

Main Menu ......................................................................................................................... 29

6.4.1 Exit .......................................................................................................................... 29

6.4.2 Auto Setup (Only Support Analog) ......................................................................... 29

6.4.3 Brightness............................................................................................................... 30

6.4.4 Contrast .................................................................................................................. 30

6.4.5 Display (Only Support Analog) ............................................................................... 30

6.4.6 Color Mode ............................................................................................................ 31

6.4.7 Clock / Phase (Only Support Analog) ..................................................................... 32

6.4.8 Audio ...................................................................................................................... 33

6.4.9 Management .......................................................................................................... 34

6.4.9.1 Scaling .................................................................................................................... 34

6.4.9.2 OSD Display ............................................................................................................ 35

6.4.9.3 Language ................................................................................................................ 35

6.4.9.4 Source .................................................................................................................... 36

6.4.9.5 Power Key Lock ...................................................................................................... 36

6.4.9.6 Recall ...................................................................................................................... 37

6.4.10 Operating Hours ..................................................................................................... 37

6.5

Supported Video Modes .................................................................................................. 38

7. Technical Specifications ................................................................................................................ 39

8. Outline Dimension ......................................................................................................................... 41

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1. Introduction

1.1

Monitor description

The equipment is applied for healthcare that is intended for general use in hospital environment

for data collection and display for reference. It shall not be used with life support system or for

medical diagnosis.

Type of equipment: Portable (on a table)

Intended location: Medical environment

Intended User Profile

Age:

Adult (Age above 21)

Gender:

Can be use by all genders

Linguistic/ Cultural Background:

At least English

Education/ Professional Competence:

General level of education

Intended User Group:

Hospital staff

Knowledge Base:

User should possess basic medical knowledge

1.2

Box of contents

 23.8” LCD Touch Screen Monitor

 AC Power Cord

 Audio Cable

 DP Cable

 VGA Cable

 DVI-HDMI Cable

 USB Cable (for touch version)

 Power Adapter (Delta 24V)

(Optional)

4 / 47

1.3

Product overview

Front View

The image below shows the front view of the display.

4

Image 1-1 Front view

1.

P-CAP touch

2.

Bezel

3.

LED

1

2

3

5 / 47

Side View

The image below shows the control keys located in the right bottom corner of the display.

4

Image 1-2 Control Key

1.

Menu / Enter key / Scrolling key

1

6 / 47

Rear View

Image 1-3 Rear view

1.

Rear cover

2.

IO cover

3.

Monitor stand

4.

Hinge cover

1

3

4

2

7 / 47

Available Connections

Image 1-4 Available connections (bottom view)

1. USB

2. RS232

3. Audio

4. Display Port

5. DVI

6. VGA

7. POWER

8.

1

3

4

5

6

2

7

8

1

3

4

5

6

7

2

8

9

8 / 47

2. Important Information

2.1

Safety information

General recommendations

Read the safety and operating instructions before operating the device.

Save the safety and

operating instructions for future reference.

Adhere to all warnings on the device and in the operating instructions manual.

Follow all

instructions for operation and use.

Electrical Shock or Fire Hazard

To prevent an electrical shock or fire hazard, do not remove the cover.

No serviceable parts are inside. Refer servicing to qualified personnel.

Do not expose this

apparatus to rain or moisture.

Modifications to the unit:

Do not modify this equipment without authorization of the manufacturer.

Degree of safety (flammable anesthetic mixture):

Equipment is not suitable for use in the presence of a flammable anesthetic mixture of air,

oxygen

,

or nitrous oxide.

Non-patient care equipment

•

Equipment primarily for use in a health care facility. It is intended for use when contact

with a patient is unlikely (no applied part).

•

The equipment may not be used with life support equipment.

•

The user should not touch the equipment, nor its signal input ports (SIP)/signal output ports

(SOP) and the patient at the same time.

Mission critical applications

We strongly recommend for there to be a replacement monitor immediately available in

mission critical applications.

Power connection – Equipment with internal power supply

•

This equipment must be grounded.

•

Power requirements: The equipment must be powered by the DC mains voltage.

•

The equipment is intended for continuous operation.

9 / 47

Power cords:

•

Do not overload wall outlets and extension cords as this may result in fire or electric shock.

•

Main leads protection (U.S.: Power cord): Power cords should be routed so that they are

not walked upon or pinched by items placed upon or against them. Pay particular attention

to cords at plugs and receptacles.

•

The power supply cord should be replaced by the designated operator only at all time.

•

Use a power cord that matches the voltage of the power outlet, which should be approved

and in compliance with the safety standard of your particular country.

•

Avoid placing the monitor near places that is hard to reach or difficult to disconnect the

power supply cord.

•

“WARNING: To avoid risk of electric shock, this equipment must only be connected to a

supply mains with protective ground”

Grounding reliability

Grounding reliability can only be achieved when the equipment is connected to an equivalent

receptacle.

Liquids and moisture

Never expose the monitor to liquids or moisture.

Never use the monitor near water - e.g. near a bathtub, washbasin, swimming pool, kitchen

sink, laundry tub or in a wet basement.

Ventilation

Do not cover or block any ventilation openings in the cover of the set. When installing the

device in a cupboard or another closed location, heed the necessary space between the set

and the sides of the cupboard.

Installation

Place the device on a flat, solid, and stable surface that can support the weight of at least 3

devices. If you use an unstable cart or stand, the device may fall, causing serious injury to a

child or adult, and serious damage to the device.

Accessory equipment connected to the analog and digital interfaces must be in compliance

with the respective nationally harmonized IEC standards (i.e. IEC 60601-1 for medical

equipment.) Furthermore all configurations shall comply with the system standard in IEC

60601-1. Anyone who connects additional equipment to the signal input part or signal output

part is configuring a medical system, and is therefore, responsible that the system complies

with the requirements of the system standard IEC 60601-1. The unit is for exclusive

interconnection with IEC 60601-1 certified equipment in the patient environment and IEC

60XXX certified equipment outside of the patient environment.

10 / 47

2.2

Environmental information

Disposal Information

Waste Electrical and Electronic Equipment

This symbol on the product indicates that under the European Directive 2012/19/EU,

governing waste from electrical and electronic equipment, this product must not be disposed of

with other municipal waste. Please dispose of your waste equipment by handing it over to a

designated collection point for the recycling of waste electrical and electronic equipment. To

prevent possible harm to the environment or human health from uncontrolled waste disposal,

please separate these items from other types of waste and recycle them responsibly to promote

the sustainable reuse of material resources.

For more information about recycling of this product, please contact your local city office or

your municipal waste disposal service.

11 / 47

2.3

Regulatory information

Indications for use

The monitor (23.8” Touch Screen LCD monitor) is applied for healthcare that is intended for

general use in hospital environment for data collection and display for reference.

FCC class B

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.

This device 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 device 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 device does

cause harmful interference to radio or television reception, which can be

determined by

turning the device off 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 device and receiver.

•

Connect the device to an outlet on a circuit different from that to which the receiver is

connected.

•

Consult the dealer or an experienced radio/TV technician for help.

Canadian notice

This ISM device complies with Canadian ICES-003.

Cet appareil ISM est conforme à la norme NMB-003 du Canada.

12 / 47

2.4

Equipment Symbols

Electrical and electronic equipment symbols

Indicates the device meets the requirements of the applicable EC directives.

Indique que l'appareil satisfait aux exigences des directives CE en vigueur.

Indicates compliance with Part 15 of the FCC rules

Indique la conformité à la partie 15 des règles de la FCC.

Indicates the device is approved according to the TUV regulations for

Canada

and US

Indique que l'appareil est approuvé conformément à la réglementation TUV

pour le Canada et les États-Unis.

Indicates the USB connectors on the device

Indique les connecteurs USB sur le périphérique.

Indicates the Display Port connectors on the device.

Indique les connecteurs du port d'affichage sur l'appareil.

Indicates the legal manufacturer.

Indique le fabricant légal.

Indicates the manufacturing date.

Indique la date de fabrication.

Temperature limit (for Transport/Storage)

Limite de température (pour le transport / stockage)

Storage humidity range(for Transport/Storage).

Plage d'humidité de stockage (pour le transport / stockage)

Atmospheric Pressure(for Transport/Storage).

Pression atmosphérique (pour le transport / stockage)

Indicates the device serial number

Indique le numéro de série de l'appareil.

Indicates the device part number or catalog number

Indique le numéro de référence de l'appareil ou le numéro de catalogue.

Warning: dangerous voltage

AVERTISSEMENT : Tension dangereuse

13 / 47

Caution

ATTENTION

Consult accompanying documents.

Consultez les documents accompagnés.

Indicates this device must not be thrown in the trash but must be recycled,

according to the European WEEE (Waste Electrical and Electronic

Equipment)

directive.

Indique que cet appareil ne doit pas être jeté à la poubelle mais doit être

recyclé, conformément à la directive européenne DEEE (déchets

d'équipements électriques et électroniques).

Indicates Direct Current (DC)

Indique le courant continu (DC).

Indicates Alternating Current (AC)

Indique le courant alternatif (AC).

Stand-by or power indicator.

Indicateur de veille ou d'alimentation.

Power ON. Power connection to the mains.

Allumer. Raccordement électrique au réseau.

Power OFF

Éteindre.

Protective earth (ground)

Protection par mise à la terre (masse).

Equipotentiality. Connect device to a potential equalization conductor.

Équipotentialité. Raccordez l'appareil à un conducteur de liaison

équipotentielle.

14 / 42

3. Cleaning the Display

3.1

Cleaning instructions

To clean the display

Cleaning the display using a sponge, cleaning cloth, or soft tissue with lightly moistened

recognized cleaning product for medical equipment. Read and follow all labeled instructions on

the cleaning product. In case of doubt about a certain cleaning product, use plain water.

CAUTION:

 Take care not to damage or scratch the front glass or LCD. Be careful with

rings or

other jewelry and do not apply excessive pressure on the front glass or LCD.

 Do not apply or spray liquid directly to the display as excess liquid may cause

damage

to internal electronics. Instead, apply the liquid to a cleaning sponge, cloth, or tissue.

ATTENTION :

 Veillez à ne pas endommager ou rayer la vitre avant ou l'écran LCD. Soyez prudent

lorsque vous portez des bagues ou autres bijoux et n'appliquez pas une pression excessive sur

le verre avant ou l'écran LCD.

 N'appliquez ou ne vaporisez pas de liquide directement sur l'écran car l'excès de liquide

peut endommager l'électronique interne. Appliquez plutôt le liquide sur une éponge, un

chiffon ou un mouchoir en papier.

15 / 42

3.2

EMC notice

Electromagnetic emissions

The monitor is intended for use in the electromagnetic environment specified below. The

customer or the user of the monitor should assure that it is used in such an environment.

Emissions test

Compliance

Electromagnetic environment –

Guidance

RF emissions

CISPR 11

Group 1

The monitor uses RF energy only for its

internal function.

Therefore, its RF

emissions are

very low and are not likely

to

cause any interference with nearby

electronic equipment.

RF emissions

CISPR 11

Class B

The monitor is suitable for use in all

establishments, including

domestic

establishments and

those directly

connected to the

public low-voltage

power supply

network that supplies

buildings

used for domestic purposes.

Harmonic emissions

IEC 61000-3-2

N/A (power

consumption less

than 75W)

Voltage fluctuations/ flicker

emissions

IEC 61000-3-3

Complies

16 / 42

Electromagnetic immunity

The monitor is intended for use in the electromagnetic environment specified below. The

customer or the user of the monitor should assure that it is used in such an environment.

Immunity test

IEC 60601 Test levels

Compliance level

Electromagnetic

environment –

guidance

Electrostatic

discharge

(ESD)

IEC 61000-4-2

± 8kV contact

± 15kV air

± 8kV contact

± 15kV air

Floors should be wood,

concrete or ceramic tile.

If floors are covered with

synthetic material, the

relative humidity should

be at least 30%

Electrical fast

transient/burst

IEC 61000-4-4

± 2kV for power supply

lines

± 1kV for input/

output

lines

± 2kV for power

supply

lines

± 1kV for input/

output

lines

Mains power quality

should be that of a typical

commercial or hospital

environment

Surge

IEC61000-4-5

± 1 kV line(s) to line(s)

± 2 kV line(s) to earth

± 1 kV line(s) to line(s)

± 2 kV line(s) to earth

Mains power quality

should be that of a typical

commercial or hospital

environment

Voltage dips,

short

interruptions

and voltage

variations on

power

supply

input lines

IEC 61000-4-11

0% residual voltage for

0.5 cycle.

0% residual voltage for

1 cycle.

70% residual voltage

for,

0.5s.

0% residual voltage for

5s.

0% residual voltage

for

0.5 cycle.

0% residual voltage

for

1 cycle.

70% residual voltage

for,

0.5s.

0% residual voltage

for 5s.

Mains power quality

should by that of a typical

commercial or hospital

environment. If the

user

of the RGP2422AMI

requires continued

operation during power

mains interruptions, it is

recommended that the

RGP2422AMI be powered

from an uninterruptible

power supply or a battery.

Power

frequency

(50/60 Hz)

magnetic field

IEC 61000-4-8

30 A/m

Not applicable

Power frequency

magnetic fields should

be

at levels characteristic

of

a typical location in

a

typical commercial or

hospital environment.

17 / 42

Immunity test

IEC 60601 Test levels

Compliance level

Electromagnetic environment

–

guidance

Conducted RF

IEC 61000-4-6

Radiated RF

IEC 61000-4-3

3 V at 0,15 - 80MHz

6 V at ISM bands

10 V/m at 80-2, 700MHz.

And 9-28V/m at 385-

6,000MHz, Pulse Mode:

27 V/m at 385MHz

28 V/m at 450MHz

9V/m at 710/745/780MHz

28 V/m at

810/870/930MHz

28 V/m at

1720/1845/1970MHz

28 V/m at 2450MHz

9V/m at

5240/5500/5785MHz

3 V at 0,15 - 80MHz

6 V at ISM bands

10V/m at 80-2,700MHz.

And 9-28V/m at 385-

6,000MHz, Pulse Mode:

27 V/m at 385MHz

28 V/m at 450MHz

9V/m at 710/745/780MHz

28 V/m at

810/870/930MHz

28 V/m at

1720/1845/1970MHz

28 V/m at 2450MHz

9V/m at

5240/5500/5785MHz

Portable and mobile RF

communications

equipment

should be

used no closer to

any

part of the monitor,

including cables, than

the

recommend

separation distance calculated

from the equation applicable

to the frequency

of the

transmitter.

Recommended

separation distance

d = 1.2√P

d = 1.2√P 80 MHz to 800

MHz

d = 2.3√P 800 MHz to 2.5

Ghz

Where P is the maximum

output power rating of the

transmitter in

watts (W)

according

to the transmitter

manufacturer and d

is the

recommended

separation

distance in

meters (m).

Field strengths from

fixed

RF transmitters,

as

determined by an

electromagnetic site

survey,

5

should be less

than the compliance

level

in each frequency range.

6

Interference may occur in

the

vicinity of equipment

marked

with symbol:

At 80 MHz and 800 MHz, the higher frequency range applies.

These guidelines may not apply in all situations. Electromagnetic propagation is affected by

absorption and reflection from structures, objects, and people.

18 / 42

Recommended separation distance

The monitor is intended for use in an electromagnetic environment in which radiated RF

disturbances are controlled. The customer of the user of the monitor can help prevent

electromagnetic interference by maintaining a minimum distance between portable and

mobile RF communications equipment (transmitters) and the monitor as recommended below,

according to the maximum output power of the

communications equipment.

Rated maximum output

power of transmitter

W

Separation distance according to frequency of transmitter

150kHz to 80MHz

d=1.2√P

80MHz to 800MHz

d=1.2√P

800MHz to 2.5GHz

d=2.3√P

0.01

0.12

0.23

0.1

0.38

0.73

1

1.2

2.3

10

3.8

7.3

100

12

23

NOTE 1：UT is the a.c. mains voltage prior to application of the test level.

NOTE 2：At 80 MHz and 800 MHz, the higher frequency range applies.

NOTE 3：Guidelines regarding conducted disturbances induced by RF fields or radiated RF fields may not apply

in all situations. Electromagnetic propagation is affected by absorption and reflection from structures,

objects and people.

NOTE 4：The ISM (industrial, scientific and medical) bands between 0.15 MHz and 80 MHz are 6.765 MHz to

6.795 MHz; 13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz .

The amateur radio bands between 0.15 MHz and 80 MHz are 1.8 MHz to 2.0 MHz, 3.5 MHz to 4.0 MHz,

5.3 MHz to 5.4 MHz, 7 MHz to 7.3 MHz, 10.1 MHz to 10.15 MHz, 14 MHz to 14.2 MHz, 18.07 MHz to

18.17 MHz, 21.0 MHz to 21.4 MHz, 24.89 MHz to 24.99 MHz, 28.0 MHz to 29.7 MHz and 50.0 MHz to

54.0 MHz.

a. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless telephones and land

mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted

theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an

electromagnetic site survey should be considered. If the measured field strength in the location in which the

monitor is used exceeds the applicable RF compliance level above, the monitor should be observed to verify

normal operation. If abnormal performance is observed, additional measures may be necessary, such as

reorienting or relocating the monitor .

b. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 10 V/m.

Recommended separation distances between portable and mobile RF communications equipment

and the monitor

The monitor is intended for use in an electromagnetic environment in which radiated RF

disturbances are controlled. The customer or the user of the monitor can help prevent

electromagnetic interference by maintaining a minimum distance between portable and mobile RF

communications equipment (transmitters) and the monitor as recommended below, according to

the maximum output power of the communications equipment.

Immunity to proximity fields from following RF wireless communication equipment has been

confirmed:

Test

frequency

(MHz)

Bandwidth

a)

(MHz)

Service

a)

Modulation

b)

Maximum

power

(W)

Minimum

separation

distance (m)

IEC/EN60601

test level

(V/m)

Compliance

level

(V/m)

385

380-390

TETRA400

Pulse

modulation

b)

1.8

0.3

27

450

430-470

GMRS 460,

FRS 460

FM

±5 kHz

deviation

1 kHz sine

2

0.3

28

19 / 42

710

704-787

LTE Band 13,

17

Pulse

modulation

b)

217 Hz

0.2

0.3

9

745

780

810

800-960

GSM 800 /

900,

TETRA 800,

iDEN 820

CDMA 850,

LTE Band 5

Pulse

modulation

b)

18 Hz

2

0.3

28

871

930

1720

1700-1990

GSM 1800;

CDMA 1900;

GSM 1900;

DECT;

LTE Band 1, 3,

4, 25;

UMTS

Pulse

modulation

b)

217 Hz

2

0.3

28

1845

1970

2450

2400-2570

Bluetooth,

WLAN,

802.11 b/g/n,

RFID 2450,

LTE Band 7

Pulse

modulation

b)

217 Hz

2

0.3

28

5240

5100-5800

WLAN

802.11 a/n

Pulse

modulation

b)

217 Hz

0.2

0.3

9

5500

5785

• For some services, only the uplink frequencies are included.

• The carrier shall be modulated using a 50 % duty cycle square wave signal.

At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

These guidelines may not apply in all situations. Electromagnetic propagation is affected by

absorption and reflection form structures, object and people.

20 / 42

CAUTION

1. The unit is for exclusive interconnection with IEC 60XXX certified equipment outside of patient

environment and IEC 60601-1 certified equipment inside the patient environment.

2. This device complies with EN60601-1-2, To minimize the interference from other equipment, a minimum

0.5 m distance shall be kept form other potential electromagnetic sources, such as the Cell Phone.

3. The power cable connector is the primary means of detaching the system from the power supply. The

monitor should be installed close to a power outlet, which is easily accessible.

4. Handle with care when transporting. Save packaging for transporting.

5. AC power inlet is considered as Disconnect Device.

6. To prevent fire or shock hazards, do not expose this unit to rain or moisture. Also, do not use this unit’s

polarized plug with an extension cord receptacle or other outlets unless the prongs can be fully inserted.

7. Do not modify this equipment without authorization of the manufacturer.

8. To prevent the risk of electric shock, make sure power cord is fully disengage the power to the unit. Please

disconnect the power cord from the AC outlet.

9. To prevent electric shock, please do not remove cover or any internal components. Refer to a qualified

technician for service.

10. This device is intended to be used (1) outside the “patient vicinity” area or (2) within the “patient

vicinity” to the patient such as consulting rooms.

11. To avoid risk of electric shock, this equipment must only be connected to a supply mains with protective

ground.

12. The LCD monitor become heat when it’s working, please do not touch the panel and plastic enclosure

over 10 seconds, and do not touch the mental enclosure on the back of the LCD monitor over 1 second.

13. For safety reasons, turn-off the power switch and unplug the monitor before cleaning.

14. Equipment with SIP/SOP connectors should either comply with IEC 60601-1 and/or IEC 60601-1-1

harmonized national standard or the combination should be evaluated.

15. The power cable connector is the primary means of detaching the system from the power supply. The

monitor should be installed close to a power outlet, which is easily accessible.

16. AC power inlet is considered as Disconnect Device.

17. To prevent fire or shock hazards, do not expose this unit to rain or moisture. Also, do not use this unit’s

polarized plug with an extension cord receptacle or other outlets unless the prongs can be fully inserted.

18. Do not modify this equipment without authorization of the manufacturer.

19. To prevent the risk of electric shock, make sure power cord is fully disengage the power to the unit. Please

disconnect the power cord from the AC outlet.

20. To avoid risk of electric shock, this equipment must only be connected to a supply mains with protective

ground.

21. Power cord shell be connected to a socket-out with earthing connection

22. CAUTION: Double pole, neutral fusing.

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