1
USES:
• To assist and maintain proper patient positioning to offload the sacrum and control body heat and moisture.
• To assist with the repositioning of a patient.
INTENDED CARE SETTINGS:
Intended to be used in hospitals, healthcare facilities, and other environments where repositioning of partially–dependent or dependent
patients is desired. This equipment is intended to be used for purposes stated in this manual. Any other use is prohibited.
INDICATIONS:
Use for patients who are dependent or partially-dependent and unable to participate in their own repositioning.
CONTRAINDICATIONS:
Patients who have thoracic, cervical, or lumbar fractures should not use the Prevalon AirTAP System (the “System”) unless a clinical
decision has been made by your facility. The equipment should not be used for patients that exceed the 550 lbs / 250 kg weight limit.
PRIOR TO USE:
Perform a visual inspection of the System. Examine the AirTAP System Glide Sheet (the “Glide Sheet”), Prevalon Air Pump (the “Air Pump”),
and/or AirTAP System Booster Pump (the “Booster Pump”) for damage or wear that is potentially hazardous and could cause the System to
malfunction. If such damage is present, DO NOT USE. Examine the power cord for damage. If the power cord is damaged, DO NOT USE the Air
Pump / Booster Pump, as a damaged power cord may cause serious injury. Ensure all parts are present. If any parts are missing, DO NOT USE.
IMAGING:
The Glide Sheet with Microclimate Body Pad is MR safe by rationale. The device is made from all non-metal materials; therefore, MR safety
testing was not performed. Compatibility tests did not show artifacts. Based on rationale, the Glide Sheet with Microclimate Body Pad is
electronically non-conductive and non-magnetic.
The Air Pump / Booster Pump are not MR safe. Please follow your facilities protocol for using the Air Pump / Booster Pump in a MR environment.
Prevalon
™
™
Patient Repositioning System
2
i
CAUTION:
• Periodically check product for signs of wear. Replace if product is damaged.
• DO NOT launder any component of the System.
• DO NOT plug Air Pump / Booster Pump into the bed.
• Glide Sheet for single patient use only.
i
WARNINGS:
Failure to comply with this Manual could result in injury or equipment malfunction.
Alterations or modifications to the System can affect the safety and functionality of the System and are strictly prohibited.
Read and understand the entire Manual before using the system.
To reduce the risk of fire or injury:
• Always follow your facility’s safe patient handling policies and procedures.
• Patient repositioning should always be performed using at least two caregivers.
• DO NOT use the Glide Sheet to lift patients.
• To avoid potential skin injury, prevent patient’s heels and head from dragging across the bed during repositioning.
• To prevent injury or accidental inflation, ensure patient is not in contact with the Valve or Hose.
• DO NOT use the Air Pump / Booster Pump in the presence of flammable anesthetics or other flammable gases or vapors.
• DO NOT store or use the Air Pump / Booster Pump outdoors.
• DO NOT use the Air Pump / Booster Pump near water.
• DO NOT cover or block any openings on the Air Pump / Booster Pump.
• DO NOT tamper with or make any adjustments to any part of the Air Pump / Booster Pump.
• DO NOT let the Air Pump / Booster Pump cord hang over the edge of a table or counter.
• DO NOT operate the Air Pump / Booster Pump if it has a damaged cord or plug, if it is not working properly, or if it has been
damaged or dropped. Contact Sage Products at 800.323.2220 for repair or replacement.
• DO NOT immerse the Air Pump / Booster Pump cord or plug in water.
• Keep cord away from heated surfaces.
• The Air Pump / Booster Pump has been designed for use exclusively with the Sage air assisted technology products.
• DO NOT use Air Pump / Booster Pump during transport.
• The Glide Sheet is not intended to secure a patient to a support surface. Follow facility policies and procedures for securing patients
to a support surface. (e.g. Trendelenburg)
