Barco MUIP-2112 User guide

Brand: Barco

Model: MUIP-2112

Type: User guide

ENABLING BRIGHT OUTCOMES

User Guide

12.5” LCD User Interface

MUIP-2112

Registered office: Barco NV

President Kennedypark 35, 8500 Kortrijk, Belgium

www.barco.com/en/support

www.barco.com

Barco NV

Beneluxpark 21, 8500 Kortrijk, Belgium

www.barco.com/en/support

www.barco.com

3K5902132 (451920612534) /03 MUIP-2112

1 Welcome!.......................................................................................................................................................................................................... 5

1.1 What's in the box ................................................................................................................................................................................6

1.2 Product overview................................................................................................................................................................................6

2 Installatie...........................................................................................................................................................................................................9

2.1 Kabelaansluitingen.........................................................................................................................................................................10

2.2 Kabelgeleiding.................................................................................................................................................................................. 11

2.3 Installatie bureausteun (optioneel)........................................................................................................................................12

3 Onderhoud...................................................................................................................................................................................................15

3.1 Gepland onderhoud.......................................................................................................................................................................16

3.2 Reinigen...............................................................................................................................................................................................16

4 Important information.........................................................................................................................................................................17

4.1 Safety information...........................................................................................................................................................................18

4.2 Informatie over het milieu ...........................................................................................................................................................21

4.3 Biologische gevaren en terugname......................................................................................................................................23

4.4 Regulatory information.................................................................................................................................................................23

4.5 EMC-kennisgeving.........................................................................................................................................................................24

4.6 Verklaring van de symbolen......................................................................................................................................................27

4.7 Juridische disclaimer.....................................................................................................................................................................30

4.8 Technical specifications...............................................................................................................................................................30

Inhoud

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5K5902132 (451920612534) /03 MUIP-2112

Introduction

The MUIP-2112 computing Touch Screen Module is a smart 12.5” display. it is released with or without

Windows OS (the units provided with Windows OS have the sticker license applied on to the rear side). Its

ruggedized design, compact size and touch-screen interface makes it suitable for system control applications.

The MUIP-2112 is not intended to be a portable device. The internal battery (if present) is foreseen mainly to

prevent the operative-system from crashing in case of momentary drop of the mains power. The internal

battery capacity could maintain the unit to work for a time of about one hour, maximum. In the normal

application of MUIP-2112 installed in a system on a VESA-arm or a desktop-support with power-supply and

LAN-cables connected, the internal battery is constantly maintained at full-charge, and is not submitted to

frequent charge-discharge cycles.

Waarschuwingen, voorzorgsmaatregelen, opmerkingen en tips

Er zijn vier niveaus voor voorzorgsmaatregelen of adviezen die in deze gebruikershandleiding worden

gebruikt. In afnemende volgorde van belang zijn dat:

WAARSCHUWING: Beschrijft een gevaar dat kan resulteren in persoonlijk letsel of de dood.

OPGELET: Beschrijft een gevaar dat het product kan beschadigen.

Geeft extra informatie over het beschreven onderwerp.

Geeft extra advies over het beschreven onderwerp.

Welcome! 1

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1.1 What's in the box

Overview

• MUIP-2112 12.5” Computing Touchscreen Module

• Power supply 19V 65W AC-DC external unit (depending on model)

• Two mains power cords (EU and US versions) (depending on model)

• 1 x user guide

Bewaar de oorspronkelijke verpakking goed. Ze werd speciaal voor dit beeldscherm ontworpen en

vormt de ideale bescherming tijdens transport en bewaring.

1.2 Product overview

Front

13 2

Afbeelding 1–1

1. MUIP-2112

2. Power Button:

Push short to turn the equipment ON/OFF.

3. Desktop support (optional)

Welcome!

7K5902132 (451920612534) /03 MUIP-2112

Back

43 5 6 7 8 9 10 11

Afbeelding 1–2

1. Rear cover fixation screw holes (2x)

2. Rear cover (standard open / optional closed version)

3. Reset Button (activation with the aid of a pin/staple)

4. Audio Microphone Input Jack

5. Audio Line Output stereo jack

6. Video Output mini DP++ interface (for connecting an external DP or HDMI monitor)

7. 1 x USB 2.0 port Type A connector

8. 1 x USB 3.0 port Type A connector

9. Gigabit Ethernet Connector (LAN1)

10.Gigabit Ethernet Connector (LAN2)

11. Power jack input connector (range 12–24Vdc, nominal 19Vdc)

12.VESA 75 mm mounting screw holes (4x)

13.Strain-relief cable (depending on model – designed according to customer specifications)

Welcome!

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Welcome!

9K5902132 (451920612534) /03 MUIP-2112

WAARSCHUWING: Lees alle belangrijke veiligheidsinformatie alvorens uw monitor te installeren

en te bedienen. Zie het relevante hoofdstuk in deze gebruikershandleiding.

WAARSCHUWING: Om deze apparatuur te installeren is voldoende expertise vereist. Alle

apparaten en de volledige configuratie moeten worden getest voor ze in gebruik worden genomen.

OPGELET: Wanneer het beeldscherm wordt gemonteerd in een medisch systeem, besteed dan de

nodige aandacht aan de bevestiging van alle kabels om te voorkomen dat ze ongewenst los komen

te zitten.

OPGELET: De apparatuur is niet bedoeld om te worden gesteriliseerd.

Installatie 2

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2.1 Kabelaansluitingen

Openen en sluiten van de achterklep

1. Verwijder de twee rubberen doppen die de bevestigingsschroeven afdekken.

2. Verwijder de twee bevestigingsschroeven en verwijder de achterklep van de MUIP-2112.

Afbeelding 2–1

3. Om de achterklep goed te sluiten, dient u eerst de kabels goed te geleiden, zoals omschreven staat in

“Kabelgeleiding”, pagina 11. Plaats de achterklep en volg bovenstaande stappen in omgekeerde volgorde.

Stroom- en LAN-aansluiting

De MUIP-2112 computer-touchscreenmodule die als een intelligente gebruikersinterface functioneert, wordt

meestal op het systeem aangesloten via een Ethernet LAN-aansluiting en/of USB-interface-aansluiting.

1. Steek de stroomstekker in de stroomstekkerhouder.

Afbeelding 2–2

2. Steek de LAN-stekker in de LAN-stekkerhouder.

Afbeelding 2–3

Installatie

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Andere kabelaansluitingen voorbeeld (alleen de uitvoering met de open achterklep)

1. Sluit de USB 3.0-stekker aan op de USB 3.0-stekkerhouder.

Afbeelding 2–4

2.2 Kabelgeleiding

Uitvoering open achterklep

De kabels kunnen op twee manieren gerouteerd worden:

1. Routeer de kabels recht omlaag (zoals hieronder afgebeeld).

Afbeelding 2–5

2. Routeer de kabels achter de pin (zoals hieronder afgebeeld).

Installatie

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Afbeelding 2–6

Deze manier van routeren kan alleen bij maximaal drie kabels.

Uitvoering gesloten achterklep (optioneel)

1. Omdat de LAN- en de stroomkabels beide omsloten worden door de trekontlastingkabel, die gerouteerd is

door het vierkante gat in de gesloten achterklap, is geen specifieke routering nodig.

Afbeelding 2–7

2.3 Installatie bureausteun (optioneel)

Richting

In de verpakking van de MUIP-2112 W00 kan een bureausteun inbegrepen zijn. Deze steun kan in twee

richtingen gemonteerd worden, zodat het scherm in verschillende hoeken geplaatst kan worden.

Installatie

13K5902132 (451920612534) /03 MUIP-2112

Afbeelding 2–8

Installatie

1. Plaats de bureausteun in de gewenste richting.

2. Monteer de MUIP-2112 op de bureausteun in liggende richting.

3. Plaats de vier VESA 75 mm montageschroeven en schroef ze vast.

Afbeelding 2–9

Installatie

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Afbeelding 2–10

Installatie

15K5902132 (451920612534) /03 MUIP-2112

Onderhoud 3

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3.1 Gepland onderhoud

Informatie

De MUIP-2112 vergt geen gepland onderhoud of kalibratie. Neem in geval van onduidelijkheid contact op met

Barco Healthcare.

3.2 Reinigen

WAARSCHUWING: Trek de stroomkabel uit de voedingsingang voor u het beeldscherm reinigt.

OPGELET: Let erop dat u het voorglas of LCD niet beschadigt of krast. Wees voorzichtig met

ringen of andere juwelen en oefen geen overmatige druk uit op het voorglas of LCD.

OPGELET: Breng vloeistof niet rechtstreeks aan op het beeldscherm, want overtollige vloeistof kan

schade veroorzaken aan de inwendige elektronica. Breng de vloeistof aan op een reinigingsdoek.

Het beeldscherm reinigen

Reinig het beeldscherm met een spons, reinigingsdoek of zacht papieren doekje, licht bevochtigd met een

erkend reinigingsproduct voor medische apparatuur. Lees en volg alle labelinstructies op het

reinigingsproduct. Gebruik bij twijfel over een bepaald reinigingsproduct gewoon water.

Mogelijke reinigingsoplossingen:

• 70 % isopropylalcohol

• 1.6 % waterige ammoniak

• Cidex® (2.4 % glutaaraldehyde-oplossing)

• Natriumhypochloriet (bleekwater) 10 %

• "Groene zeep" (USP)

• 0.5 % chloorhexidine in 70 % isopropylalcohol

• Like Cleansafe® optische reinigingsvloeistof

Gebruik de volgende producten niet:

• Alcohol/oplosmiddelen in een concentratie > 70%

• Sterke alkalische logen, sterke oplosmiddelen

• Zuren

• Detergenten met fluoride

• Detergenten met ammoniak met een concentratie van > 1.6 %

• Detergenten met schurende middelen

• Staalwol

• Spons met schurende middelen

• Stalen messen

• Doek met staaldraad

Onderhoud

17K5902132 (451920612534) /03 MUIP-2112

Important

information

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4.1 Safety information

Algemene aanbevelingen

Lees de veiligheids- en bedieningsinstructies grondig voor u het apparaat bedient.

Bewaar de veiligheids- en bedieningsinstructies, zodat u later nog iets kunt opzoeken.

Leef alle waarschuwingen op de apparatuur en in de instructiehandleiding na.

Volg alle instructies voor bediening en gebruik.

Gevaar voor elektrische schokken of brand

Om elektrische schokken of brandgevaar te voorkomen, mag u de behuizing niet verwijderen.

In het toestel zitten geen onderdelen die moeten worden bediend. Laat onderhoudswerken over aan

gekwalificeerd personeel.

Stel dit apparaat niet bloot aan regen of vocht.

Wijzigingen aan de eenheid

Wijzig deze apparatuur niet zonder toestemming van de fabrikant.

Type of protection (electrical):

Monitor provided with external power supply: Class II equipment.

Monitor provided without external power supply: Class I or II, depending from the Class of the external power

supply used.

Degree of safety (flammable anesthetic mixture):

Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or

nitrous oxide.

The equipment is not operable if the air oxygen content is above 25%.

Non-patient care equipment

• Equipment primarily for use in a health care facility, including the patient area.

• The equipment should not be used with life support equipment.

• The user should not touch the signal input ports (SIP) / signal output ports (SOP) and the patient at the

same time. The rear cover must be kept closed and screwed.

Mission critical applications

We strongly recommend to immediately have a replacement display available in mission critical applications.

Use of electrical surgical knives

Provide as much distance as possible between the electrosurgical generator and other electronic equipment

(such as monitors). An activated electrosurgical generator may cause interference with this equipment and

can disrupt the functionality of the display.

Power connection

• Power requirements: The equipment must be powered using medical approved AC/DC power supply .

• The medical approved AC/DC power supply must be powered by the AC mains voltage.

• The power supply is specified as a part of the ME equipment or combination is specified as an ME system.

• The equipment should be installed near an easily accessible wall socket.

• To disconnect the main power, unplug the AC adapter.

• The equipment is intended for continuous operation.

• The compliance of the equipment with the Medical Safety and EMC requirements has been evaluated with

the provided medical grade power supply. If a different power supply is used, further investigation for

Safety and EMC requirements have to be performed at system level.

Important information

19K5902132 (451920612534) /03 MUIP-2112

• Do not use the supplied AC adapter for powering other devices.

• Do not move the equipment while the power cord and connection cables are connected. Otherwise,

damage to the equipment, power cord and connection cables, fire or an electric shock may result.

Transient over-voltage

To fully disengage the power from the device, please disconnect the power cord from the AC inlet.

Connections

Any external connection with other peripherals must follow the requirements of clause 16 of IEC60601-1 3rd.

Ed. or Table BBB.201 of IEC 60601-1-1 for the medical electrical systems.

To maintain compliance with EMC Regulation, use only shielded interface cables for the connection to

peripheral devices.

Power cords:

• Please use the power cord provided with this equipment. If a power cord is not supplied with this

equipment, please contact your supplier. For all other cases, please use a power cord that matches the AC

voltage of the power outlet and has been approved by and complies with the safety standard of your

particular country.

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

• Mains lead protection: Power cords should be routed so that they are not likely to be walked upon or

pinched by items placed upon or against them, paying particular attention to cords at plugs and

receptacles.

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

Liquids and moisture

Never expose the equipment to liquids or moisture.

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

tub or in a wet basement.

The equipment is IPx3 compliant. The power supply is IPx0.

Moisture condensation

Do not use the equipment under rapidly changing temperature and humidity conditions or avoid direct contact

with cold air from air-conditioning outlet.

Moisture may condense on the surface or inside of the equipment, or create a mist residue inside the

protection plate. This is not a malfunction of the product itself, although it may cause damage to the

equipment.

If condensation exists, leave the equipment unplugged until there is no condensation.

Ventilation

When installing the device in a cupboard or another enclosed location, heed the necessary space between the

set and the sides of the cupboard.

The LCD panel becomes warm during operation. This is not a malfunction. Allow adequate air circulation to

reduce the temperature of the equipment.

Installation

• Place the equipment on a flat, solid and stable surface that can support the weight of at least 3 units. If you

use an unstable cart or stand, the equipment may fall, causing serious injury to a child or adult and/or

serious damage to the equipment.

• Do not allow to climb or rest on the equipment.

• When the equipment is attached to an arm, do not use the equipment as a handle or grip in order to move

the equipment. Please refer to the instruction manual of the arm for instructions on how to move the arm

with the equipment.

• Provide full attention to safety during installation, periodic maintenance and examination of this equipment.

Important information

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• Sufficient expertise is required for installing this equipment, especially to determine the strength of the wall,

arm or ceiling suspension for withstanding the display’s weight. Be sure to entrust the attachment of this

equipment to the wall to a duly skilled technician and pay adequate attention to safety during the

installation and usage.

• The manufacturer is not liable for any damage or injury caused by mishandling or improper installation.

• When the display is assembled in the medical system, take care of unwanted detachment.

• The equipment should be installed near an easily accessible place. Do not install or leave the unit in places

subject to extreme temperatures, near a radiator, heating vent, or in places subject to mechanical vibration

or shock. Subjecting the LCD display to extreme temperatures, could cause deformations of the casing or

malfunctions.

• Avoid to place the unit near any equipment that generates a strong electro-magnetic field, such as surgical

knife or other medical appliances.

• Avoid places subject to inordinate amounts of dust, dirt, or sand, for example near an open window or an

outdoor exit.

• If setting up temporarily in an outdoor environment, be sure to take adequate precautions against airborne

dust and dirt. Otherwise unrecoverable malfunctions could occur.

Handling

Do not press on or scratch the front protection screen. Do not place a heavy object on the equipment.

If the equipment is used in a cold place, a residual image may appear in the screen. This is not a malfunction.

The screen returns to normal as the temperature rises to a normal operating level.

If a still picture is displayed for a long time, a residual image may appear for a while. The residual image will

eventually disappear.

Transportation

Disconnect the cable from the equipment when transporting.

When you transport the equipment, hold it firmly in both hands. If you drop the equipment, you may be injured

or the equipment may be damaged.

When you transport the equipment for repair or shipment, use the original cardboard box and packing

materials.

Batteries

• This device uses an RTC battery (Mod. CR-2032) and a Lithium Ion battery pack (Mod. BN2012350-

001LPA-01). Both batteries are not user-replaceable. Do not attempt to replace them, contact Barco

authorized repair facilities.

• Batteries used with this equipment have been tested for compatibility and should only be replaced with

approved parts.

• The batteries are not designed to be charged by any other electrical source. Charging could generate gas

and internal short-circuiting, leading to distortion, leakage, overheating, explosion, or fire.

Connection of PEMS by network/data coupling to other equipment

• Connection of the PEMS to a network/data coupling that includes other equipment could result in

previously unidentified risks to patients, operators or third parties.

• The responsible organization should identify, analyze, evaluate and control these risks.

• Subsequent changes to the network/data coupling could introduce new RISKS and require additional

analysis.

• Changes to the NETWORK/DATA COUPLING include:

- Changes in NETWORK/DATA COUPLING configuration;

- Connection of additional items to the NETWORK/DATA COUPLING;

- Disconnecting items from the NETWORK/DATA COUPLING;

- Update of equipment connected to the NETWORK/DATA COUPLING;

- Upgrade of equipment connected to the NETWORK/DATA COUPLING.

General warnings

• All devices and complete setup must be tested and validated before taking into operation.

• At end user application level, it is necessary to foresee a backup unit in case the equipment fails.

Important information

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Barco MUIP-2112 User guide

Brand: Barco

Model: MUIP-2112

Type: User guide

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Nederlands: Barco MUIP-2112 Gebruikershandleiding

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