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K5902132 (451920612534) /03

MUIP-2112

18

4.1 Safety information

General recommendations

Read the safety and operating instructions before operating the device.

Retain 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 electric shock or fire hazard, do not remove cover.

No serviceable parts 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.

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.

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

Important information

Содержание MUIP-2112

Страница 1: ...ENABLING BRIGHT OUTCOMES User Guide 12 5 LCD User Interface MUIP 2112...

Страница 2: ...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...

Страница 3: ...support installation optional 12 3 Maintenance 15 3 1 Scheduled maintenance 16 3 2 Cleaning 16 4 Important information 17 4 1 Safety information 18 4 2 Environmental information 21 4 3 Biological haz...

Страница 4: ...K5902132 451920612534 03 MUIP 2112 4...

Страница 5: ...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...

Страница 6: ...pending on model Two mains power cords EU and US versions depending on model 1 x user guide Keep your original packaging It is designed for this display and is the ideal protection during transport an...

Страница 7: ...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 E...

Страница 8: ...K5902132 451920612534 03 MUIP 2112 8 Welcome...

Страница 9: ...pter in this user guide WARNING Sufficient expertise is required to install this equipment All devices and complete setup must be tested before taking into operation CAUTION When the display is assemb...

Страница 10: ...cover first route the cables as described in Cable routing page 11 Install the rear cover and follow the above steps in reverse order Power and LAN connection The MUIP 2112 Computing Touch Screen Mod...

Страница 11: ...rsion only 1 Connect the USB 3 0 connector to the USB 3 0 input Image 2 4 2 2 Cable routing Open rear cover version The cables can be routed in two different ways 1 Route the cables straight downwards...

Страница 12: ...th enclosed by the strain relief cable which is routed through the square hole in the closed rear cover no specific routing is needed Image 2 7 2 3 Desktop support installation optional Orientation A...

Страница 13: ...112 Image 2 8 Installation 1 Place the desktop support in the desired orientation 2 Install the MUIP 2112 on the desktop support in landscape orientation 3 Install and tighten the four VESA 75 mm moun...

Страница 14: ...K5902132 451920612534 03 MUIP 2112 14 Image 2 10 Installation...

Страница 15: ...15 K5902132 451920612534 03 MUIP 2112 Maintenance 3...

Страница 16: ...eaning cloth To clean the display Clean the display using a sponge cleaning cloth or soft tissue lightly moistened with a recognized cleaning product for medical equipment Read and follow all label in...

Страница 17: ...17 K5902132 451920612534 03 MUIP 2112 Important information 4...

Страница 18: ...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 cr...

Страница 19: ...aundry 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 av...

Страница 20: ...t 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 cardb...

Страница 21: ...patients The MUIP 2112 has no essential performances and the provided Windows OS is not a class A software CAUTION The enclosure has to be checked upon collision damage refer to qualified service per...

Страница 22: ...o o o o Fan o o o o o o Paper Manuals o o o o o o CD manual o o o o o o SJ T 11364 This table is prepared in accordance with the provisions of SJ T 11364 o GB T 26572 o Indicates that this toxic or h...

Страница 23: ...edition of the ANSI AAMI ST35 standard on each single failed Product that is returned for servicing repair reworking or failure investigation to Seller or to the Authorized Service Provider At least...

Страница 24: ...chnician for help Changes or modifications not expressly approved by the party responsible for compliance could void the user s authority to operate the equipment FCC responsible Barco Inc 3059 Premie...

Страница 25: ...ifferent from that to which the receiver is connected Consult the dealer or an experienced technician for help Electromagnetic immunity The MUIP 2112 is tested to be used in the electromagnetic enviro...

Страница 26: ...commercial or hospital environment Conducted RF IEC 61000 4 6 3 Vrms 6 Vrms in ISM bands 150 kHz to 80 MHz 3 Vrms 6 Vrms in ISM bands Radiated RF IEC 61000 4 3 3 V m 80 MHz to 2 7 GHz 10 V m Immunity...

Страница 27: ...57 Indicates the device is approved according to the UL Recognition regulations E346057 MEDICAL GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL SHOCK FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH ANS...

Страница 28: ...ed according to the INMETRO regulations Indicates the USB connectors on the device Indicates the DisplayPort connectors on the device yy xx Indicates the temperature limitations3 for the device to saf...

Страница 29: ...that it should be carried with two persons Indicates that the box should not be cut with a knife a cutter or any other sharp object 20 C 60 C xx yy Indicates the temperature limits4 to which the devic...

Страница 30: ...ssor SoC Intel Celeron N2930 Quad Core 1 83GHz 2MB Cache BIOS INSYDE Operating System Microsoft Windows 7 Embedded Windows 10 ioT Networking Built in Gigabit Ethernet LAN interfaces 2 ports Memory 4 G...

Страница 31: ...0601 1 14 Medical Electrical Equipment Part 1 General Requirements for Basic Safety and Essential Performance Harmonized with Ed 3 1 IEC 60601 1 2 2014 EN 60601 1 2 2015 EN 55011 CISPR11 Class B FCC C...

Страница 32: ...sktop support Dimensions W x H x D 312 x 200 x 37 mm Certifications compliance China CCC Europe CE ITE DEMKO US and Canada UL FCC ICES 003 Standards IEC 60601 1 2012 Edition 3 1 Medical electrical equ...

Страница 33: ...20612534 03 MUIP 2112 Image 4 1 Code number 12NC or K code Model No Serial number 72yyww000000 72 Original code FIMI yy Year ww Week 01 to 52 Manufacturer Date 000000 6 digits progressive number Impor...

Страница 34: ...K5902132 451920612534 03 MUIP 2112 34 Important information...

Страница 35: ......

Страница 36: ...Barco NV Beneluxpark 21 8500 Kortrijk Belgium Registered office Barco NV President Kennedypark 35 8500 Kortrijk Belgium www barco com K5902132 451920612534 03 2020 11 18...

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