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Good visual ergonomics and image quality in order to improve the working environment for the
user and to reduce sight and strain problems. Important parameters are luminance, contrast,
resolution, reflectance, colour rendition and image stability.
• Energy-saving mode after a certain time – beneficial both for the user and the environment
• Electrical safety
• Electromagnetic fields
• Noise emissions
• The product must be prepared for recycling and the manufacturer must have a certified
environmental management system such as EMAS or ISO 14 000
• Restrictions on
o chlorinated and brominated flame retardants and polymers
o heavy metals such as cadmium, mercury and lead.
The requirements included in this label have been developed by TCO Development in cooperation
with scientists, experts, users as well as manufacturers all over the world. Since the end of the
1980s TCO has been involved in influencing the development of IT equipment in a more user-
friendly direction. Our labelling system started with displays in 1992 and is now requested by
users and IT-manufacturers all over the world.
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In accordance with UL 2601-1/IEC 60601-1, the product is cssified as Continuous duty Class I
equipment, which is not protected against ingress of liquids. The product is not suitable for use in
the presence of a flammable anaesthetic mixture with air or with oxygen or nitrous oxide.
This equipment has been tested and found to comply with the limits for medical devices to the IEC
601-1-2:1994. These limits are designed to provide reasonable protection against harmful
interference in a typical medical installation. This equipment generates, uses and can radiate radio
frequency energy and, if not installed and used in accordance with the instructions, may cause
harmful interference to other devices in the vicinity. However, there is no guarantee that
interference will not occur in a particular installation. If this equipment does cause harmful
interference to other devices, which can be determined by turning the equipment 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 device.
Increase the separation between the equipment.
Connect the equipment into an outlet on a circuit different from that to which the other device
(s) are connected.
Consult the manufacturer or field service technician for help.
Video In / RS 232 / Video Out
Accessories equipment connected to the analog and digital interfaces must be certified to the
respective IEC standards (i.e. IEC 950 for data processing equipment and IEC 601-1 for medical
equipment.) Furthermore all configurations shall comply with the system standard IEC 601-1-1.
Everybody who connects additional equipment to the signal input part or signal output part
configures a medical system, and is therefore, responsible that the system complies with the
requirements of the system standard IEC 601-1-1. If in doubt, consult the technical services
department or your local representative.
Transport and Storage Limitations:
Temperature Range of -40°C to +70°C
Relative Humidity of 10 -95%, non-condensing
* Bio-accumulative is defined as substances which accumulate within living organisms.
** Lead, Cadmium and Mercury are heavy metals which are Bio-accumulative.
This manual is suitable for devices