Service and Claims .............................................................................. 22
Declaration of Conformity ..................................................................23
1
Warnings and Cautions
Please read this manual and follow its instructions carefully. The words
warning, caution, and note carry special meanings and should be
carefully reviewed:
arningThe personal safety of the patient or physicia n may be
involved. Disregarding this information could result in
injury to the patient or physician.
arningA lightning bolt within a triangle is intended to warn of
the presence of hazardous volt age. Refer all servic e to
authorized personnel.
autionSpecial service procedures or precautions must be
followed to avoid damaging the instrument.
NoteSpecial information to make maintenance easier or
important information more clear.
Warnings
WarningTo avoid potential serious injury to the user and the
patient, and/or damage to this device, the user must:
1. Restrict this device to use by, or on the order of, a physician,
because of Federal law (United States of America).
2. Read the operating manual thoroughly and be familiar with its
contents prior to using this equipment.
3. Carefully unpack the unit and check if any damage occurred
during shipment.
4. Test this equipment prior to a surgical procedure. This monitor
was fully tested at the factory before shipment.
5. Do not place the monitor or any other heavy object on the power
cord. Damage to the cable can cause fire or electric shock.
6. Should any solid object or liquid fall into the panel, unplug the unit
and have it checked by qualified personnel before operating it
any further.
7. Unplug the unit if it is not to be used for an extended period of
time. To disconnect the cord, p ull it out by the plu g. Never pull the
cord itself.
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8. To avoid electric shock, avoid removing control unit covers.
9. Do not attempt internal repairs or adjustments not specifically
detailed in this operating manual.
10. Pay close attention to the care and cleaning instructions in this
manual. A deviation may cause damage (refer to the Cleaning
section).
11. Do not sterilize the monitor.
12. Use appropriate caution to prevent contact with fluids, if the unit is
being used with a power supply in patient environments.
Cautions
1. The AC Adapter must be plugged into a grounded power outlet.
2. Use only the proprietary VISIONELECT (model 240-030-930)
power supply (model 240-030-931) for the VISIONELECT (model
240-030-930) monitor. Make a proper connection by ensuring
that the shrink tubing completely secures the connection between
the DC power cord and the extension cord.
3. Grounding reliability can only be achieved when the equipment is
connected to an equipment receptacle labeled “Hospital Only” or
“Hospital Grade.”
4. To connect to an international power supply, use an attachment
plug appropriate for the power outlet.
5. Turn power off when unit is not in use.
6. Remove the power module and connection when transporting the
unit.
7. Save the original carton and associated packing material. They
will be useful should you have to transport or ship the unit.
8. Handle the monitor with care. Do not strike or scratch the screen.
9. Never operate the unit right after having been transported from a
cold location directly to a warm location.
10. Do not expose the monitor to moisture or directly apply liquid
cleaners directly to the screen. Spray the cleaning solutio n into a
soft cloth and clean gently.
11. Allow adequate air circulation to prevent internal heat buildup.
12. Do not place the unit on surfaces (rugs, blankets, etc.) or near
materials (curtains, draperies) that may b lock the ventilat ion slots.
The monitor is cooled by natural convection and has no fan.
13. Do not install the unit near sunlight, excessive dust, mechanical
vibration or shock.
English
EN
3
14. The unit is designed for operation in a horizontal position. Do not
operate the unit in a vertical position.
15. Keep the unit away from equipment that uses strong magnets
(i.e., large loudspeakers).
16. Do not touch the patient with signal input or output connectors.
Equipment with SIP/SOP connectors should either comply with
IEC 60601-1 and/or IEC 60601-1-1 harmonized national
standards or the combination should be evaluated.
17. CAUTION: Changes or modifications not expressly approved by
the party responsible for compliance could void the user's authority
to operate the equipment.
NOTE : This equipment has been tested and found to comply
with the limit for a Cass B digital device, pursuant to Part 15 of
the FCC Rules. These limits are designed to provide resonable
protection against harmful interference in a residential 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 radio
communications. However, there is no guarantee that
interference will not occur in a particular installation, which can
be determined by turning the equipment off and on, the user is
encourage to try to correct the interference by one or more of
the following measures.
• Reorient or relocate the receiving device.
• Increase the separation distance between the equipment.
• Connect the equipment to 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.
18. To ensure electromagnetic compatibility, refer to the
“Electromagnetic Compatibility” section of this manual. The
VISIONELECT (model 240-030-930) monitor must be installed
and operated according to the EMC information provided in this
manual.
The VISIONELECT (model 240-030-930) monitor has been tested under
the UL 60601-1 standard and is UL listed for medical application.
The warranty is void if any of these warnings or cautions are
disregarded.
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Symbol Definitions
The following symbols appear on the product, its labeling, or the product
packaging. Each symbol carries a special definition, as defined below
Dangerous: High Voltage
Consult accompanying documents.
Direct Current
Indicates protective earth ground.
For indoor use only.
DC power control switch
English
EN
SN
51LJ
Medical Equipment
E215822
Serial Number
Top - Bottom
Fragile
Do not get wet
Maximum Stacking
Manufacturer
European Authorized Representative
Indicates proof of conformity to applicable European Economic Community
Council directives and to harmonized standards pub lished in the of ficia l journal
of the European Communities.
Tested and certified by DEMKO in accordance with EN 60601-1 and
EN 60601-1-2.
Medical Equipment is in accordance with UL 60601-1 and CAN/CSA C22. 2 No.
601.1 in regards to electric shock, fire hazards, and mechanical hazards.
Tested to comply with FCC Class B standards.
This symbol indicates that the waste of electrical and electronic equipment
must not be disposed as unsorted municipal waste and must be collected
separately. Please contact the manufacturer or other authorized disposal
company to decommission your equipment.
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Product Description and
Intended Use
The VISIONELECT (model 240-030-930) 21-Inch High Definition LCD
Monitor is an intelligent, microprocessor-based TFT-LCD monitor
intended for use in endoscopic surgical applications. It has an
ergonomically designed display and is compatible with most analog RGB
(Red, Green, Blue) display standards.
The VISIONELECT (model 240-030-930) monitor has the following
features:
• Advanced Viewing Solution (AVS): A sophisticated filter
extends the viewing angle of the screen image, without
sacrificing contrast ratio and brightness.
• Upgraded video cards or software will not require buying a new
monitor because of the wide auto-scanning compatibility range.
• The internal microprocessor digitally controls auto-scanning, for
horizontal scan frequencies between 31.47 KHz and 78.88 KHz,
and vertical scan frequencies between 50.0 Hz and 85.1 Hz. In
each frequency mode, the microprocessor-based circuitry allows
the monitor to function at the precision of a fixed frequency.
• The resident memory allows for storing factory default settings
and also additional user adjustment parameters.
• The maximum resolution achievable is UXGA (1600 × 1200,
be60Hz),st suited for Stryker cameras.
• The monitor is compliant with the VESA-DPMS power-
management standard. In order to save energy, the monitor
must be connected to a system compliant with the standard.
• The monitor is designed to mount an accessory (such as a
camera or speaker) with a 2 lbs (max) load per hole.
• The monitor is certified by UL International in accordance with
medical standard UL 60601-1. It is also CE marked for sale in
the European Community for integration or use with medical
products. It is certified by DEMKO according to EN 60601-1
and EN 60601-1-2 for sale to the medical market.
Product Contents
1. Carefully unpack the VISIONELECT (model 240-030-930)
monitor. Save the original carton and associated packing
material. They will be useful should you have to transport or ship
the unit.
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