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10
Introduction
Introduction
Thank you for purchasing BenQ displays. Please read this manual carefully for proper use. Keep
this user manual in a safe place for easy reference when needed.
In this user manual the steps needed to reach a menu are shown in condensed form, for
example:
Display
>
Brightness
.
Features
•26" wide-screen LCD (IPS-Pro LCD technology)
•Provide high brightness, high contrast and full HD resolution images.
•True 16:9 HDTV aspect ratio, ideal for use with HD endoscopic cameras.
•Widest range of SD and HD input signals, including 3G-SDI and DisplayPort.
•Maximum ten (10) settings can be set as preset.
•Easy cleaning design with sealed front (IPX3).
•Lightweight for easy mounting on spring arms.
Intended use
The SE series displays are intended for use in a medical environment to display high quality
video and graphic images from cameras or other compatible medical imaging systems, other
than diagnostic X-ray equipment. This product is capable of displaying Radiology (PACS) images
for reference, not diagnostic purposes. These devices cannot be used in digital mammography
and life-support system. These devices are designed for exclusive interconnection with
IEC60601-1-1 certified equipment.
Equipment connected to the analog or digital interfaces must comply with the respective IEC
standards (e.g. IEC 60950-1 or data processing equipment and IEC 60601-1 for medical
equipment). Furthermore all configurations shall comply with the current version of the
standard for SYSTEMS IEC 60601-1 everybody who connects additional equipment to the signal
input part or signal output part configure a medical system, and is therefore responsible that
the system complies with current version of the requirements of the system standard
IEC60601-1 doubt, consult the technical service department or your local representative.
Classification
•Type of protection against electric shock: Class 1
•The degree of protection against electric shock: No Applied Part.
•The degree of protection against the ingress of water: IPX3 (only for the front side)
•The mode of operation: Continuous Operation
The equipment is not suitable for use in the presence of a flammable anesthetic mixture with air
or with oxygen or nitrous oxide: Not AP or APG Category.