Use Instructions
Table Of Contents
- Introduction
- Indications For Use
- Contraindications For Use
- For Use With
- Accessories
- System Overview
- User/Patient Safety
- Features
- Physical Buttons
- Graphical user interface
- Definitions
- Instructions
- Inspection and Maintenance
- Cleaning
- Storage and Handling
- Disposal/Recycle
- Troubleshooting
- Error Messages
- Specifications
- Electromagnetic Compatibility
- Appendix
SL5019 Rev. A
9
Low Suction
• LOW SUCTION HAZARD
NOT FOR USE as a suction source for the following applications:
•
Organ stabilizer/positioner devices
•
Patient positioner devices
Death or serious injury can result from fluctuating suction levels.
High Suction
• HIGH SUCTION DEVICE [MAX = 528 mmHg/70kPa]
• The effectiveness of aspiration is dependent upon the intensity of the vacuum applied.
• ALWAYS use the minimum suction setting required to achieve the desired clinical outcome.
• ALWAYS follow your institution’s guidelines for suction limits.
• DO NOT connect directly to chest tubes.
• DO NOT connect to closed wound drains.
• DO NOT connect directly to tracheal tubes.
• NOT FOR USE as a suction source for intermittent suction applications.
Death or serious injury can result from improper suction levels.
• The suction setting may only be adjusted by the SUCTION SETTING on the touch display. Interruption and
restoration of rover power, whether accidental or intentional, does not reset the suction setting to zero.
Electrical Safety
• Use only AMSINO-approved system components and accessories, unless otherwise specified. Using other
electronic components and accessories may result in increased electromagnetic emissions or decreased
electromagnetic immunity of the system.
• Take special precautions regarding electromagnetic compatibility (EMC) when using medical electrical
equipment like this system. Install and place this system into service according to the EMC information
contained in this manual. See the Specifications section
• This equipment utilizes mobile RF communications equipment that can affect medical electrical equipment.
• Please take attention that changes or modification not expressly approved by the party responsible for
compliance could void the user’s authority to operate the equipment.
• This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:
(1) This device may not cause harmful interference, and
(2) This device must accept any interference received, including interference that may cause undesired
operation.
• This device complies with Industry Canada licence-exempt RSS standard(s). Operation is subject to the