Nihon Kohden medical TEC-5602 Defibrillator parts Load Test Board
UR-0484 6190-909671A S 13
► Brief Introduction
This device is intended for medical use by qualified personnel
only. Use only products approved by Nihon Kohden with this
technique. Use of unapproved products or in an unapproved manner
may affect product performance specifications. This includes but is
not limited to batteries, paper, pens, extension cords, electrodes,
input and power boxes.
This type of technology is commonly used in various applications
such as remote controls, wireless devices and data transmission
between electronic devices.
| No | code No | QTY | Description |
| 7 | UR-0484 | 1 | TEST LOAD BOARD |
► Features
This equipment/or system is IEC 60601-1-2 International Standard
Electromagnetic Hunting Electrical equipment support / or system
treatment. us, electromagnetic field No interference is allowed if
the goods or levels covered by IEC 601-1-2 are excluded
equipment/or system and equipment/ system is frictionless Make the
outside. Therefore, team/or system work overlaps with each other
What not to ask, avoid, stay electromagnetic equipment while
continuing to operate the equipment and/or system.
Type of protection against electrical shock
• When connecting to an AC power (commercial use): Class I ME
equipment
• When not connecting to an AC power (commercial use): Internally
powered ME equipment Degree of protection against electrical shock
• Type BF applied parts: External paddles, disposable pads
• Type CF applied parts: Internal paddles, internal paddles (with
switch)
• Defibrillation-proof type CF applied parts: ECG connection cable,
electrode leads, SpO2 probes, CO2 sensor kit Protection against
harmful ingress of water or fine particulate
• IP44: TEC-5621 and TEC-5631 with a pad adapter or internal
paddles, TEC-5611
• IP41: TEC-5621 and TEC-5631 with external paddles, TEC-5601,
TEC-5602 Applicable when connecting all patient cables (except the
recorder) Sterilization or disinfection methods specified by
manufacturers
• Internal paddles, internal paddles with switch: High-pressure
steam sterilization (autoclave sterilization), plasma gas
sterilization, ethylene oxide gas sterilization (EOG sterilization)
• Except internal paddles and internal paddles (with switch): Not
for sterilization Qualifications for use in a high-oxygen
atmosphere Not qualified Safety level for use in air and flammable
anesthetic gas or oxygen/nitrous oxide and flammable anesthetic gas
Not applicable Mode of operation Continuous operation Installation
conditions Indoor and in-vehicle uses Frequency of use (class by
IEC 60601-2-4: 2010) High frequent use
► How to use
1.Use with other tools.
In equipment, when the equipment and/or system is adjacent to or
installed with other equipment
and/or the system may affect other devices. Check the device and/or
system before use
Northerners operate with different equipment.
2.Use of unspecified accessories, conductors and/or cables:
When accessories are not specified, connectors and/or cables are
attached to the instrument and/or cable
The system may increase electromagnetic emissions or decrease
electromagnetic immunity.
The specific configuration of the device and/or electromagnetic
system is implemented
Requirements with specific configurations. Only with these devices
and/or systems
3.Use the undefined configuration:
When devices and/or systems are used with unspecified system
configurations
EMC test configurations may result in increased or decreased
electromagnetic emissions
Electrical Immunity Only use this device and/or system with proper
configuration.
