Viasys sipap user manual

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Remove Subscription Confirm Remove. Forums Documents Videos News. Follow Us. Request a quote. Request Parts. Add to My Bench. This warranty does not cover normal maintenance such as cleaning, adjustment or lubrication and updating of equipment parts.

This warranty shall be void and shall not apply if the equipment is used with accessories or parts not manufactured by the Company or authorized for use in writing by the Company or if the equipment is not maintained in accordance with the prescribed schedule of maintenance. The warranty stated above shall extend for a period of One 1 year from date of shipment, with the following exceptions:. Components for monitoring of physical variables such as temperature, pressure, or flow are warranted for ninety 90 days from date of receipt.

Elastomeric components and other parts or components subject to deterioration, over which the Company has no control, are warranted for sixty 60 days from date of receipt. Internal batteries are warranted for ninety 90 days from the date of receipt. The foregoing is in lieu of any warranty, expressed or implied, including, without limitation, any warranty of merchantability, except as to title, and can be amended only in writing by a duly authorized representative of the Company.

Revision History List of Figures List of Tables Chapter 1 - Product Description Chapter 2 - Product Specifications Chapter 3 - Summary of Warnings and Cautions Chapter 5 - Operation Chapter 6 - Operating Modes Chapter 7 - Alarms and Indicators Chapter 9 — Explanation of Symbols Appendix A - Product Configurations Appendix B - Pneumatic Diagram Appendix C - Alarm Troubleshooting Appendix D - Fault Management Figure 1 — Stand unpacking and assembly Figure 2 — Stand and Driver assembly Figure 4 — Attaching the Abdominal Respiratory Sensor Figure 5 — Flow Pressure Nomogram Figure 6 — Front Panel Figure 7 — Rear Panel Figure 8 — Set Up Screen Figure 10 — Mode Select Screen Figure 11 — Parameter Adjust Screens Figure 12 — Main Screen Figure 13 — Monitored Parameters Screen Figure 15 — BiPhasic Figure 16 — BiPhasic tr Figure 17 - Flat Battery screen Table 1 — Functions and Accessories Table 2 - Soft-key operation Table 3 — Parameter Default Value Table 4 — Alarm Symbols and Indicators Table 5 — Equipment Symbols Table 6 — Button Symbols Table 8 — US Configuration Parameters Table 9 — Alarm Troubleshooting Table 10 — Fault Classification Table 11 — Fault Recovery This equipment radiates and is susceptible to radio frequency energy.

If not installed and used in accordance with the instructions in this manual, electromagnetic interference may result. The equipment has been tested and found to comply with the limits set forth in BS EN for Medical Electrical Equipment Part General requirements for safety-collateral standard. Electromagnetic compatibility — requirements and tests.

These limits provide reasonable protection against electromagnetic interference when operated in the intended use environments e. This device is also designed and manufactured to comply with the following standards:.

This equipment contains electromagnetic components whose operation can be affected by intense electromagnetic fields. Do not operate this device in a MRI environment or in the vicinity of high-frequency surgical diathermy equipment, defibrillators, or short-wave therapy equipment. Electromagnetic interference could disrupt the operation of the device. The system is for use in Hospitals, Hospital Type facilities and intra-Hospital transport environments and is indicated for the treatment of Newborn and Infant patients.

Federal law restricts the sale of this device except by or on order of a physician. Reuse of single-patient use accessories may degrade the performance of the product or cause cross contamination. Equipment is not suitable for use in presence of flammable anesthetics. If you have a question regarding the Declaration of Conformity for this product, please contact CareFusion.

It can also be used when transporting these patients within the hospital environment. This system has been designed and tested to perform optimally when used only with accessories available from CareFusion.

These accessories include circuits and generators, prong and mask patient interfaces and bonnets. NCPAP — continuous positive airway pressure based on clinician set pressure. BiPhasic — time triggered pressure assists are delivered based on clinician set Time-High, rate and pressure criteria. Battery Backup — Up to 2 hours of battery backup allows for intra-hospital transport.

Clear indicators are provided for power supply in use AC or DC , and battery charge level. Screen Lock — After seconds of no screen inputs, the screen changes to the Locked Screen to prevent inadvertent changes. Upon activation of a high priority alarm the screen changes to an unlocked state to allow access to controls. Klausner, James F. Pediatric Pulmonology ; Khalaf Nabeel, M. Configuration Parameters. Attempting to operate this equipment without fully understanding its features and functions may result in unsafe operating conditions.

Warnings and Cautions, which are general to the use of the device under all circumstances, are included in this section. Some Warnings and Cautions are also inserted within the manual where they are most meaningful.

Notes are also located throughout the manual to provide additional information related to specific features. If you have a question regarding the installation, set up, operation, or maintenance of the device, contact CareFusion see page v.