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9
Storage and Operating Environment Guidelines
Avoid damp locations. Do not operate and store the device beyond the specified limits. Do not
operate the device with wet hands.
Do not expose the device to direct sunlight during storage.
Do not store the device in areas with highly fluctuating temperatures.
Do not store the device close to heating equipment and appliances.
Do not store the device near sources of vibration.
Do not store and operate the device in locations that are exposed to chemicals, explosive gas
and solvents.
Keep the device away from dusty environments.
There are no user serviceable parts inside the RESCUE 230. Only authorized service personnel
should open the device for repairs.
During recharging, when the device is connected and disconnected from the mains power
connector, hold the plug and not the electrical cord.
Operating environmental condition limits:
Temperature: 0 °C to 50 °C
Relative Humidity: 5 % to 95 % (non-condensing)
Storage environmental condition limits:
Temperature: -20 °C to 70 °C
Relative Humidity: 5 % to 95 % (non-condensing)
Electrical Safety Guidelines
Use the only the original power supply during recharging. See the section Chapter on Power
Supplies for more details.
During recharging, do not place the device where the environmental conditions exceed the
storage conditions specified in the Storage and Operating Environment Guidelines
Do not use the RESCUE 230 if it has been submerged in water. Call
immediately for service assistance.
During operation, the device should be placed away from sources
of electromagnetic interference such as motors, generators, X-Ray
equipment, radio transmitters, cellular mobile telephones and
others, as these might interfere with the signals being acquired.
The RESCUE 230 is classified as follows:
- It is a Class II, BF equipment in terms of electrical shock
prevention (EN 60601-1). It is not proper to operate this device
around combustible anesthetic or solvents.
- For the ECG patient cable is a Class II, CF (EN60601-1).
- The Electromagnetic emission level is Class B according to EN
60601-1 (Safety of Electric Medical Equipment), and the noise
redemption is B level according to the EN 60601-1-2
(Electromagnetic Compatibility Requirements).