natus Olympic Brainz Monitor, Справочное руководство

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Brainz BRM3 Brain Monitor Reference Manual |
8
Introduction
Loading of Roll Pole
The Roll Pole is designed to carry a load equal to the standard BRM3 Brain Monitor components and any
Natus-recommended optional accessories (e.g. a printer mounting bracket and printer). Do not apply a
load exceeding the sum weight of these items. Install the printer mounting bracket above the Accessory
Basket. To ensure stability, the printer mounting bracket must be mounted at least 8” (21 cm) below the
height adjustment knob.
Transporting the BRM3 Brain Monitor
Before moving the BRM3 Brain Monitor, lower the Touchscreen Monitor to its lowest position on the Roll
Pole and lock in firmly in position. If a printer is fitted, close the paper holder.
Use with high frequency electrosurgical equipment
Do not use diathermy/electrosurgery or defibrillation equipment on a patient while they are connected to
the BRM3 Brain Monitor. This may cause interference to the EEG signals and could damage the device.
Disconnect the Neonatal Sensor Set from the DAU while any such procedure is being carried out.
Personal injury hazard
Ensure that the Touchscreen Monitor is securely mounted on the Roll Pole, to avoid personal injury.
Patient strangulation hazard
To minimize the risk of patient strangulation, position the DAU so as to minimize any risk of the cables
becoming wrapped around the patient’s throat.
Use of accessory equipment
Use of accessory equipment not approved by Natus Medical Incorporated, or not complying with safety
standards equivalent to those met by the BRM3 Brain Monitor, may lead to a reduced level of safety of
the resulting system or failure of the BRM3 Brain Monitor to operate correctly.
Connection to accessory equipment
Accessory equipment connected to any accessory port of the Touchscreen Monitor unit (including USB
ports) must be certified to applicable IEC standards (IEC 60950 for data processing equipment and IEC
60601-1 for medical equipment). All configurations shall comply with the medical electrical systems
standard IEC 60601-1-1. Anyone who connects additional equipment to such an accessory port part
configures a medical system, and is responsible for ensuring that the system complies with the
requirements of the medical electrical systems standard IEC 60601-1-1. If in doubt, contact an
Authorized Service Center or Natus Medical Incorporated.
Indications for servicing
If any of the following situations occurs, stop using the BRM3 Brain Monitor immediately and have it
checked by your healthcare institution’s service personnel.

The AC supply cable or attachment plug is damaged.

The equipment has been exposed to moisture.

The equipment does not work well, or does not work in the way described by this document.

The equipment has been dropped and damaged.

The equipment has obvious signs of breakage.