• To avoid potential for spread of disease or infection, single-use disposable components (e.g., electrodes)
must not be reused. To maintain safety and effectiveness, electrodes must not be used beyond their
expiration date.
• To ensure the safety of both the patient and the device, 1.5 meters (5’) of open area should surround
the patient.
• A possible explosion hazard exists. Do not use the device in the presence of a flammable anesthetic mixture
with air or with oxygen or nitrous oxide.
• Where the integrity of external protective earth conductor arrangement is in doubt, the device shall be
operated from its internal electrical power source.
• All signal input and output (I/O) connectors are intended for connection of only those devices complying
with IEC 60601-1, or other IEC standards (e.g., IEC 60950) as appropriate to the device. Connecting
additional devices to the device may increase chassis and/or patient leakage currents. To maintain operator
and patient safety, consideration should be given to the requirements of IEC 60601-1-1, and leakage currents
should be measured to confirm no electric shock hazard exists.
• To improve immunity to potential interfering electromagnetic signals, shielded cabling is recommended
when connecting the device to a network.
• To maintain operator and patient safety, equipment connected to the same network as the device must meet
the requirements of IEC 60950 or IEC 60601-1.
• To prevent electric shock due to unequal ground potentials that may exist between points of a distributed
network system or fault conditions in external network connected equipment, network cable shielding
(where used) must be connected to protective earth ground appropriate to the area where the device is used.
• The device has not been designed for use with high-frequency (HF) surgical equipment and does not
provide a protective means against hazards to the patient.
• The quality of the signal produced by the device may be adversely affected by the use of other medical
equipment, including but not limited to defibrillators and ultrasound machines.
• For proper operation and the safety of users or patients and bystanders, equipment and accessories must be
connected only as described in this manual. Do not connect a telephone line cable to the LAN connector.
• This device may contain a GSM/GPRS (cellular modem) or wireless LAN (WLAN) module for transmitting
ECG records. Device labeling and the presence of an antenna port will indicate if your device is equipped
with such a module. If so equipped, the following notices apply:
• The GSM/GPRS module operates in allocated frequency bands depending on the model.
Identification of the installed GSM/GPRS module can be found on a label on the bottom of the device.
• MultiTech Systems, Inc. Model MTSMC-G-F1 (Europe and elsewhere): 900/1800 MHz
• MultiTech Systems, Inc. Model MTSMC-G-F2 (U.S. and elsewhere): 850/1900 MHz
• MultiTech Systems, Inc. Model MTSMC-G-F4 (Quad Band): 850/900/1800/1900 MHz,
user selectable
• The WLAN identification can be found on a label on the bottom of the device.
• Quatech, Inc. Model WLNG-AN-DP101: 2400 MHz
User Safety Information
(Continued)
v
Содержание ELI 150 Rx
Страница 12: ...User Safety Information Continued x...
Страница 25: ...ELI 150 Rx Left Side Figure 1 2 ELI 150 Rx Rear Figure 1 3 SECTION 1 3...
Страница 26: ...SECTION 1 ELI 150 Rx Base Figure 1 4 4 T5A 250V...
Страница 34: ...SECTION 2 12...
Страница 44: ...SECTION 3 22...
Страница 58: ...SECTION 4 36...
Страница 74: ...APPENDIX B 52...
