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.
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.
Do not modify this equipment without authorization of the manufacturer.
Periodic maintenance inspections are essential to keep the monitor in optimum condition and ensure safe operation.
With the monitor disconnected from the mains, perform the following periodic check:
General recommendations:
Equipment with external power supply: Class I equipment
Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide.
Equipment primarily for use in a health care facility that is intended for use where contact with a patient is unlikely (no applied part).
The equipment shall 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.
Equipment not suitable for use in locations where children are likely to be present.
We strongly recommend there is a replacement monitor immediately available in mission critical applications.
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 them. The interference can activate the OSD menu of the display and as such disrupt the functionality of the display.
) SELV power supply.) power supply must be powered by the AC mains voltage.To fully disengage the power to the device, please disconnect the power cord from the AC inlet.
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 well shielded interface cables for the connection to peripheral devices.
Europe: H05VV-F or H05VVH2-F PVC cord with appropriate EU plug.
US and Canada: “hospital grade” cord-set has to be used, provided with instructions to indicate that grounding reliability can be achieved only when the equipment is connected to an equivalent receptacle marked hospital only or hospital grade. These instructions need to be marked either on the equip. or on a tag on the power cord.
Do not overload wall outlets 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.
Use a power cord that matches the voltage of the power outlet, which has been approved and complies with the safety standard of your particular country.
Korea: Use KC certified products; Plug: 250 V~, 16 A; Power cord: 60227 IEC 53, 3G0.75 mm² / 60227 IEC 53, 3G1.0 mm²; Connector: 250 V~, 10 A.
Grounding reliability can only be achieved when the equipment is connected to an equivalent receptacle.
Do not use monitor under rapid temperature and humidity change condition or avoid cold air from air-conditioning outlet directly.
Moisture may condense on the surface or inside of the unit, 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 monitor.
If condensation happens, let the monitor stand unplugged until there is no condensation.
Do not cover or block any ventilation openings in the cover of the set. When installing the device in a cupboard or another enclosed location, heed the necessary space between the set and the sides of the cupboard.
Place the equipment 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 equipment may fall, causing serious injury to a child or adult, and serious damage to the equipment.
Do not allow to climb or rest on the equipment.
The monitor has been designed to be used in landscape position with a tilt of -10° (backward) and +10° (forward)
When adjusting the angle of the equipment, move it slowly so as to prevent the equipment from moving or slipping off from its stand or arm.
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.
Sufficient expertise is required for installing this equipment, especially to determine the strength of the wall for withstanding the display's weight. Be sure to entrust the attachment of this equipment to the wall to licensed contractors of Barco and pay adequate attention to safety during the installation and usage.
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 video falls away.
Barco is not liable for any damage or injury caused by mishandling or improper installation.
Disconnect the equipment’s power cord from the AC inlet and refer servicing to qualified service technicians under the following conditions:
The device has no means to be incorporated in an IT-network in the clinical environment.
The enclosure has to be checked upon collision damage, refer to qualified service personnel.
The protective screen (if present) is made of tested high-resistance glass. Nonetheless there is the possibility that it may crack if subject to strong impacts. Evaluate and prevent the risk of possible breakages of the protective screen by correctly handling and positioning the monitor in the operating room.
The monitor is intended for indoor use.
The monitor is not intended to be sterilized.
The monitor has not applied parts, but the front side of the LCD panel and the plastic enclosure have been treated as applied part because considered accidentally touchable by the patient for a time <1 minute.
Finland: "Laite on liitettävä suojamaadoituskoskettimilla varustettuun pistorasiaan"
Norway: "Apparatet må tilkoples jordet stikkontakt"
Sweden: "Apparaten skall anslutas till jordat uttag"