Vividimage® 4K Surgical Display
OPM3000, Rev. C Operation Manual 2
Notices for Users
FCC Statement
WARNING: FCC Regulations state that any unauthorized changes or modifications to this equipment
not expressly approved by the manufacturer could void the user's authority to operate this equipment.
Note: This equipment has been tested and found to comply with the limits for a Class A digital device,
pursuant to Part 15 of the FCC Rules.
These limits are designed to provide reasonable protection against harmful interference when the equipment is
operated in a commercial environment. This equipment generates, uses, and can radiate radio frequency energy
and, if not installed and used in accordance with the instruction manual, may cause harmful interference to radio
communications. Operation of this equipment in a residential area is likely to cause harmful interference in which
case the user will be required to correct the interference at his own expense.
For part numbers RLM274K and RLM314K3, use the included power supply, Astrodyne 24V 150W 6.25A Medical
Power Supply (VTPWS24V625A) with 4 ft. (1.22m) cable, or one of the external power supplies listed in
“Specifications” on page 18, designed in accordance with safety requirements of ANSI/AAMI ES60601-1:2005, to
ensure compliance with FCC regulations.
Declaration of Conformity
Vividimage® 4K Surgical Display RLM274K/RLM314K3/RLM274KNPWR/RLM314K3NPWR: This
device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device
may not cause harmful interference, and (2) this device must accept any interference received, including
interference that may cause undesired operation.
Compliant with the ANSI/AAMI ES60601-1:2005 standard:
Function, Intended Application and Mode of Operation: The Vividimage® 4K Surgical Displays are
intended to be used in hospital environments in the displaying and viewing of video and graphics for review and
analysis by trained medical practitioners. The mode of operation for this device is continuous operation.
These devices are classified as Class 1 Equipment: RLM274K/RLM314K3/RLM274KNPWR/RLM314K3NPWR.
Accessory Equipment: Accessory equipment connected to the analog and digital interfaces must be
certified to the respective IEC standards (i.e. IEC 60950 for data processing equipment and IEC 60601-1 for
medical equipment). Furthermore, all configurations shall comply with the system standard IEC 60601-1-1. Any
equipment connected to the signal input part or signal output part configures a medical system. Therefore this
equipment, and new configuration, must comply with the requirements of the system standard IEC 60601-1-1. For
a complete list of current certifications, see “Specifications” on page 18.
Manual Scope
This manual is written for use for RLM274K, RLM314K3, RLM274KNPWR, and RLM314K3NPWR. When
describing a different specification/function between the monitors, the part number is given. When the part
number is not given, the description is true for all monitors. For product appearance, illustrations of part number
RLM314K3 are used in this manual. The integrated microphone in models RLM274K, RLM314K3,
IMPORTANT: To aid in reporting in the case of loss
or theft, or for service maintenance purposes, please
record the monitor's part number and serial number in
the space provided. The numbers are located on the
back of the monitor.
Part #:
Serial #: