User manual HP M1722B CODE MASTER XL+

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[. . . ] M1722B CodeMaster XL+ Defibrillator/Monitor User's Guide QhIH &!!(#(' QvrqvVT6Er! @qvv" Notice About This Edition Publication number M1722-94980 Edition 3 Printed in USA The information in this guide applies to the CodeMaster XL+ defibrillator/monitor. Hewlett-Packard shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this material. Authorized EU-representative: Hewlett-Packard Deutschland GmbH Herrenbergerstrasse 130 D-71034 Boeblingen Germany Fax: +49-7031-14-2346 Hewlett-Packard assumes no liability for failures resulting from RF interference between HP medical electronics and any radio frequency generating equipment at levels exceeding those established by applicable standards. CAUTION Warranty Hewlett-Packard makes no warranty of any kind with regard to this material, included, but not limited to, the implied warranties or merchantability and fitness for a particular purpose. The manufacturer, importer and seller are responsible for the effects on safety, reliability and performance only if: assembly operations, extensions, re-adjustments, modifications or repair are carried out by persons authorized by them, and the electrical installation of the relevant room complies with all local regulations and the equipment is used in accordance with the instructions for use. [. . . ] Semi-disposable sensors can be reused, but the adhesive wrap must be discarded after each use. Reusable sensors can be reused on different patients. Semi-Disposable Reusable Before you start SpO 2 monitoring: 1 2 Estimate the patient's weight, and determine the best site for the sensor. Use the Sensor Guide to select the correct type and size of sensor for the identified location. To connect sensors from other manufacturers you need the HP M1900B Connector Cable. - 4 5 6-3 TP HvvtPvhy VvtTP HvhQhvr Apply the Sensor to the Patient The CodeMaster XL+ supports the use of many sensors. Follow the manufacturer's guidelines for applying and using the sensor. Application of the Reusable Sensor Avtr%! 6yvphvsurH (6SrhiyrTr 6-2 Push the sensor over the fingertip so the cable lies on the back of the hand, and secure the cable to the wrist with the wrist-strap supplied. This ensures that the light sources in the sensor lie over the base of the fingernail, giving the best measurement results. If the sensor is not in the correct position, inaccurate readings result. In extreme cases, the instrument displays dashes instead of an SpO2 reading. When correctly positioned, the end of the finger just touches the end of the sensor. 8 6V UD PI When non-HP SpO2 sensors are used, application must be consistent with the manufacturer's own guidelines. 6-4 TP HvvtPvhy VvtTP HvhQhvr X 6S I DIB Qytrqpvvvthvprhrurvxsqrvhiyr puhtrvxvpuhhprvvppuhvvhvrqqrvtiyvrvt rrrpvhvpyhyrhrhqhvrvuvhvrq rsvhqhvtvhrxvuytTrpvsvphrv irtvrrvrvrpvspuhtrvxvhyvr vphyhuhyvtrhqhhpur8urpxurhyvphvvrh rtyhvrhyhyrhrruhqpuhtrurvrvsh pvrvxvhyvuyqppHrsrrpurpxvthir rvrqqrhvqvvqhyhvrpqvv Troubleshooting Sensor Application Failure to apply the sensor properly may cause incorrect measurement of arterial oxygen saturation. Patient Movement Make sure that the application site chosen does not move excessively, which may adversely affect the performance of the sensor. You may have to replace the sensor to ensure good adhesion, or you may have to choose another application site. Inspecting the Application Site Inspect the SpO2 sensor site at least once every 2 hours to ensure adhesion, skin integrity, and correct alignment of the light emitter and photodetector. Should alterations of skin integrity occur, remove the sensor and reapply at another recommended site. Circulation at Application Site Wrapping the tape too tightly, or using supplemental tape, can cause venous pulsations that could potentially lead to inaccurate saturation measurements. Therefore, do not wrap the adhesive too tightly and do not use additional tape to 6-5 TP HvvtPvhy VvtTP HvhQhvr secure the sensor. High positive intrathoracic airway pressures, valsalva maneuvers, or other consequences of impaired venous return may also cause venous pulsations. Avoid placing the SpO2 sensor on any extremity with an arterial catheter, blood pressure cuff, or intravascular venous infusion line. Connect the Sensor to the CodeMaster XL+ When you have applied the sensor to the patient, plug the disposable and semidisposable sensors into the connector cable and plug this cable into the SpO2 socket on the lower right of the CodeMaster XL+. Plug the M1190A sensor directly into the SpO2 socket of the CodeMaster XL+. The plug is keyed and is color-coded blue to distinguish it from the white ECG socket. Avtr%" TP v 8rpvturTP Trur8qrHhrYG 6-3 6-6 TP HvvtPvhy VvtTP HvhQhvr 8 6V UD PI Do not force the SpO2 connector into the ECG input socket. Doing so may damage the pins on the cable connector. Start Monitoring Turn the defibrillator on, if necessary, by turning the Energy Select control to Monitor On. Press the right corner of the display. TP PPss button to display the SpO2 reading in the upper SpO2 Readings Avtr%# HR LEAD I I TP rhqvt SPO2 PR 72 Qyrhr Qyrhyvqrvqvph 8qrHhrYG9vyhvuTP Srhqvt 6-4 The pulse amplitude indicator shows the quality of the SpO2 signal. [. . . ] Environmental Operating Conditions: 0 to 55 C, 15 to 95% relative humidity, 15, 000 ft altitude. Environmental Storage Conditions: -20 to 70 C, 90% relative humidity for 24 hours at 65 C, 15, 000 ft altitude. A-14 DhyyhvhqTr Trpvsvphv Monitor Inputs: ECG may be viewed through paddles or patient cable. Lead Fault: LEADS OFF message and dashed baseline appear on monitor if a lead becomes disconnected. Common Mode Rejection: Greater than 100 dB measured as per AAMI standards for cardiac monitors (EC13). [. . . ]

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