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Intended Use
The MD210C2/MD210C3/MD211C2/MD211C3 Color displays are intended to be used for displaying and viewing of digital
images for diagnosis by trained physicians.
To guarantee the display performance as specifi ed, it must only be used in conjunction with NEC approved display controllers.
MD210C2/MD210C3/MD211C2/MD211C3 cannot be used for a life-support system.
This device must not be used in digital mammography.
This device is designed for exclusive interconnection with IEC 60601-1 certifi ed equipment.
Contraindications: None known.
Safety Precaution
The unit is designed for exclusive interconnection with IEC 60950-1 certifi ed equipment outside of patient environment and
IEC 60601-1 certifi ed equipment inside the patient environment.
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Equipment connected to digital interfaces must comply with the respective IEC standards (e.g. IEC 60950-1 for data
processing equipment and IEC 60601-1 for medical equipment).
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This device complies with IEC 60601-1-2. To minimize the interference from other equipment, a minimum 0.5 m distance
shall be kept from other potential electromagnetic sources, such as a cell phone.
•
To reduce the risk of electric shock, make sure the power cord is unplugged from the wall socket. To fully disengage
the power to the unit, please disconnect the power cord from the ac outlet. Do not remove the front or back cover. No
user serviceable parts inside. Refer servicing to qualifi ed service personnel. The AC outlet shall be readily available and
accessible.
This device uses temperature-controlled fans for internal cooling. The use of this device in surgery rooms is not recommended
if cleaning of the air intakes from dust and lint at regular time intervals cannot be performed by the user (maximum interval: six
months).
This device is equipped with an integrated front sensor and ambient light sensor complying with the IEC 62563-1 standard
requirements for measurement devices with a calibration traceable to a primary standards laboratory. Therefore, these sensors
can be re-calibrated using external luminance and illuminance meters as a reference, which were calibrated following country
specifi c legal obligations for metrological control. When re-calibrated in a regular manner, the integrated front sensor and
ambient light sensor may then be used for remote quality assurance following the IEC 62563-1 standard. NEC Display Solutions
recommends to check the integrated front sensor and ambient light sensor at intervals of two (2) years.
North America Customers
Grounding reliability can only be achieved when the equipment is connected to an equivalent receptacle marked "Hospital Only"
or "Hospital Grade". That signal input port need to be connected properly and that any unused signal input port shall not be
accessible for the patient to contact in the patient area after the LCD is integrated into a medical system.
Federal law restricts this device to sale by or on the order of a licensed healthcare practitioner.
European Customers
Unpacking, installation and calibration of this monitor must only be done by authorized and trained personnel. Any installation
done by a non-authorized person is done under his own risk and we accept no responsibility in any device malfunctioning.
Medical Imaging
MD210C2/MD211C2 is designed for 1200 x 1600 (portrait mode) or 1600 x 1200 (landscape mode) medical imaging.
MD210C3/MD211C3 is designed for 1536 x 2048 (portrait mode) or 2048 x 1536 (landscape mode) medical imaging.
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