ARJO Huntleigh Healthcare
KCI Therapeutics Mattress Systems
AtmosAir series Mattress Replacement Systems User Manual Rev B Feb 2011
User Manual
32 Pages
Preview
Page 1
AtmosAir™ Mattress Replacement System (MRS) User Manual
AtmosAir™ with SAT™ 4000 Series AtmosAir™ with SAT™ 9000 Series AtmosAir APod™ 25 Series AtmosAir™ with SAT™ T-Series AtmosAir™ with SAT™ V-Series
DISCLAIMER OF WARRANTY AND LIMITATION OF REMEDY KCI HEREBY DISCLAIMS ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION ANY IMPLIED WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE, ON THE KCI PRODUCT(S) DESCRIBED IN THIS PUBLICATION. ANY WRITTEN WARRANTY OFFERED BY KCI SHALL BE EXPRESSLY SET FORTH IN THIS PUBLICATION OR INCLUDED WITH THE PRODUCT. UNDER NO CIRCUMSTANCES SHALL KCI BE LIABLE FOR ANY INDIRECT, INCIDENTAL, OR CONSEQUENTIAL DAMAGES AND EXPENSES, INCLUDING DAMAGES OR INJURY TO PERSON OR PROPERTY, DUE IN WHOLE OR IN PART TO THE USE OF THE PRODUCT OTHER THAN THOSE FOR WHICH DISCLAIMER OF WARRANTY OR LIMITATION OF LIABILITY IS EXPRESSLY PROHIBITED BY SPECIFIC, APPLICABLE LAW. NO PERSON HAS THE AUTHORITY TO BIND KCI TO ANY REPRESENTATION OR WARRANTY EXCEPT AS SPECIFICALLY SET FORTH IN THIS PARAGRAPH. Descriptions or specifications in KCI printed matter, including this publication, are meant solely to generally describe the product at the time of manufacture and do not constitute any express warranties except as set forth in the written limited warranty included in this publication or with this product. Information in this publication may be subject to change at any time. Contact KCI for updates. Important Information For Users In order for KCI products to perform properly, KCI recommends the following conditions. Failure to comply with these conditions will void any applicable warranties. • Use this product only in accordance with these instructions and applicable product labeling. • Assembly, operations, extensions, re-adjustments, modifications, technical maintenance or repairs must be performed by qualified personnel authorized by KCI. Contact KCI for information regarding maintenance and repair. • Ensure the electrical installation of the room complies with the appropriate national electrical wiring standards. Specific indications, contraindications, warnings, precautions and safety information exist for KCI’s therapeutic support systems. It is important for users to read and familiarize themselves with these instructions and to consult the treating physician prior to patient placement and product use. Individual patient conditions may vary. Notice This product has been configured from the manufacturer to meet specific voltage requirements. Refer to the product information label for specific voltage.
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Table of Contents Introduction... 2 Indications ... 2 Contraindications... 2 Risks and Precautions ... 2 Safety Information ... 3
Preparation for Use... 4 Mattress Installation ... 5 AtmosAir™ with SAT™ 4000, 9000 (all models), APod™25 (all models) and T-Series (all models) ... 5 AtmosAir™ V-Series ... 5
Pump Installation ... 7 Patient Placement and Nursing Care ... 8 Alternating Pressure / Rotation Adjustment ... 8 CPR ... 9 Skin Care ... 9 Incontinence / Drainage ... 9 General Operation ... 9
Care and Cleaning ... 10 General Instructions ... 10 Cleaning Mattress During Single Patient Use ... 10 Cleaning Mattress Between Multiple Patient Uses ... 10 Cleaning Air Pump and Tubes (A and AR models) ... 11
Preventive Maintenance Schedule ... 11 Daily Cleaning... 11 Weekly Cleaning ... 11 Inspection / System Check-Out ... 11
Troubleshooting ... 12 Parts Diagram - AtmosAir™ with SAT™ 4000 ... 13 Parts Diagram - AtmosAir™ with SAT™ 9000, T-Series and V-Series ... 14 Parts Diagram - AtmosAir™ with SAT™ APod™ 25 Series ... 15 Parts Diagram - AtmosAir™ Pump (A and AR models)... 16 Replacement Parts ... 17 Specifications ... 20 Electromagnetic Compatibility... 21 Warranty ... 24 Symbols Used ... 26 Customer Contact Information ... 27
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Introduction CAUTION: It is important that you carefully read and review these instructions with your healthcare professional. If you have any questions of a medical nature, please contact your healthcare professional. This document should be saved in an easily accessible place for quick reference. It is recommended that all sections of this guide be read prior to product use. Carefully review the Contraindications, Safety Information, and Risks and Precautions sections prior to placing a patient on any AtmosAir™ with SAT™ Mattress Replacement System (MRS).
Indications • For prevention or treatment of skin breakdown
Contraindications • Unstable vertebral fracture • Cervical and skeletal traction
Risks and Precautions Transfer – Standard precautions should be taken during patient transfer. Rotation / Alternating Pressure (for A and AR models) – Prior to engaging rotation or alternating pressure, ensure that bed frame has side rails and that all side rails are fully engaged in full upright and locked position. Ensure pump hoses are properly connected to appropriate side of mattress for the desired function (see Pump Installation). WARNING: Incorrect connection of pump hoses can increase risk of potential patient falls. Side rails and Restraints – WARNING: Use or non-use of restraints, including side rails, can be critical to patient safety. Serious or fatal injury can result from the use (potential entrapment) or non-use (potential patient falls) of side rails or other restraints. See related Safety Information. Patient Migration – Specialty surfaces have different shear and support characteristics than conventional surfaces and may increase the risk of patient movement, sinking and / or migration into hazardous positions of entrapment and / or inadvertent bed exit. Monitor patients frequently to guard against patient entrapment. Oxygen Use – DANGER: Risk of explosion if used in the presence of flammable anesthetics. Use of this product’s pump in an oxygen-enriched environment may produce potential of fire hazard. This equipment is not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide. Unplug and do not use pump when using oxygen-administering equipment other than the nasal, mask, or half-bed-length tent type. Electromagnetic Interference – Although this equipment conforms with the intent of the directive 89/336/EEC in relation to electromagnetic compatibility, all electrical equipment may produce interference. If interference is suspected, move equipment away from sensitive devices or contact the manufacturer. Shock Hazard – Electrical shock hazard; do not remove pump case covers. Refer to qualified service personnel.
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Safety Information Patient Entrance / Exit – Caregiver should always aid patient in exiting the bed. Make sure a capable patient knows how to get out of bed safely (and, if necessary, how to release the side rails) in case of fire or other emergency. Brakes – Caster brakes should always be locked once the bed is in position. Verify wheels are locked before any patient transfer to or from the bed. Bed Height – To minimize risk of falls or injury, the bed should always be in the lowest practical position when the patient is unattended. Bed Frame – Always use a standard healthcare bed frame with this mattress, with any safeguards or protocols that may be appropriate. Bed frame and side rails (if used) must be properly sized relative to the mattress to help minimize any gaps that might entrap a patient's head or body. It is recommended that bed and side rails (if used) comply with the FDA's Hospital Bed System Dimensional and Assessment Guidance To Reduce Entrapment. Head of Bed Elevation – Keep head of bed as low as possible to help prevent patient migration. Side rails / Patient Restraints – Whether and how to use side rails or restraints is a decision that should be based on each patient’s needs and should be made by the patient and the patient’s family, physician and caregivers, with facility protocols in mind. Caregivers should assess risks and benefits of side rail / restraint use (including entrapment and patient falls from bed) in conjunction with individual patient needs, and should discuss use or non-use with patient and / or family. This includes assessment of the bed occupant, and the combination of bed frame, side rail and mattress (or mattresses where overlays are used). Risk assessment should be repeated if the bed frame, mattress, side rail or condition or patient changes. Consider not only the clinical and other needs of the patient but also the risks of fatal or serious injury from falling out of bed and from patient entrapment in or around the side rails, restraints or other accessories. For a description of entrapment hazards, a description of at-risk patients and guidance to further entrapment risks, refer to the FDA's Hospital Bed System Dimensional and Assessment Guidance To Reduce Entrapment and other information referenced at www.kci1.com/KCI1/safetyinformation or www.fda.gov. Consult a caregiver and carefully consider the use of bolsters, positioning aids or floor pads, especially with confused, restless or agitated patients. It is recommended that side rails (if used) be locked in the full upright position when the patient is unattended. Make sure a capable patient knows how to get out of bed safely (and, if necessary, how to release the side rails) in case of fire or other emergency. Monitor patients frequently to guard against patient entrapment. CAUTION: To help prevent inadvertent bed exit or falls, ensure the distance between top of side rails (if used) and top of mattress (without compression) is approximately 4.5 in (11.4 cm). Consider individual patient size, position (relative to the top of the side rail), and patient condition in assessing fall risk. I.V. and Drainage Tubes – I.V. and drainage tubes should always have slack for alternating pressure or rotation and other patient movements. Skin Care – Monitor skin conditions regularly and consider adjunct or alternative therapies for high acuity patients. Give extra attention to skin over any raised side bolster and to any other possible pressure points and locations where moisture or incontinence may occur or collect. Early intervention may be essential to preventing skin breakdown.
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Fluids – Avoid spilling fluids on pump controls. If spills do occur, clean fluid from pump wearing rubber gloves or while unit is unplugged to avoid any possibility of shock. Once fluid is removed, check operation of components in area of spill. Fluids remaining on controls can cause corrosion, which may cause components to fail or operate erratically, possibly producing potential hazards for patient and staff. Avoid Fire Hazards – To minimize risk of fire, connect the bed’s power cord directly into a wall-mounted outlet. Do not use extension cords or multiple outlet strips. Review and follow FDA’s Safety Tips for Preventing Hospital Bed Fires (dated 12/18/03) and other information referenced at www.fda.gov. No Smoking in Bed – Smoking in bed can be dangerous. To avoid the risk of fire, smoking in bed should never be allowed. Power Cord – Position power cord to avoid a tripping hazard and / or damage to the cord. Ensure power cord is kept free from all pinch points and moving parts and is not trapped under casters. Improper handling of the power cord can cause damage to the cord, which may possibly produce risk of fire or electric shock. General Protocols – Follow all applicable safety rules and institution protocols concerning patient and caregiver safety. Disposal – At the end of useful life, dispose of waste according to local requirements or contact the manufacturer for advice.
Preparation for Use 1.
Open shipping container(s). Do not use sharp instruments to open boxes. Damage to mattress could result.
2.
Remove AtmosAir™ with SAT™ MRS from plastic protective cover. The mattress cover may appear wrinkled when unpacked. To remove wrinkles, allow mattress up to 24 hours to accommodate; see Troubleshooting for more information. Wrinkles will not affect inflation or function, so MRS may be used immediately if needed.
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3.
Check mattress surface for tears or cracking; do not use if tears or cracks are present.
4.
If re-installing MRS onto a new frame or for a new patient, check mattress surface for staining and soiling; clean and / or disinfect as required (see Care and Cleaning).
5.
Level bed and lock brakes.
6.
Remove existing mattress from bed frame.
Mattress Installation AtmosAir™ with SAT™ Mattress Replacement Systems are not compatible with the Hill-Rom® Advanced Series frames.
AtmosAir™ with SAT™ 4000, 9000 (all models), APod™ 25 (all models), and T-Series* (all models) 1.
Position mattress on bed frame with logo facing up and product information tags at foot end of bed. Magnets are integrated on the AtmosAir™ T-Series bottom cover to help keep the mattress in place during foot section extension / retraction.
2.
Ensure mattress is properly positioned with no gaps between mattress and bed frame or side rails. Always use a standard healthcare bed frame with safeguards or protocols that may be appropriate. Frame and side rails must be properly sized relative to the mattress to help minimize any gaps that might entrap a patient’s head or body.
AtmosAir™ V-Series* 1.
2.
Position mattress on bed frame with logo facing up and product information tags at foot end of bed.
Figure 1 Locking Bar
Slide locking bar located in pocket on underside of headend of mattress to one side, as shown at right (Figure 1).
* T-Series is compatible for use with the Hill-Rom® Total Care® bed frame. V-Series is compatible for use with the Hill-Rom® VersaCare® frame. Total Care® and VersaCare® are trademarks of Hill-Rom® and / or its affiliates.
HEAD OF BED Bed Frame
Underside of Mattress
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3.
Slip end of locking bar into slot on head-end of bed frame, as shown below (Figures 2 and 3).
Figure 2
Figure 3
Locking Bar
Slot
Bed Frame
4.
Slip other end of locking bar into other slot on head-end of bed frame, as shown at right (Figure 4).
5.
Repeat steps 2 thru 4 to secure foot-end of mattress.
Locking Bar
Slot
Slot
Locking Bar
Figure 4
Foot-end locking bar may need to be flexed slightly to slip into foot-end slots.
Magnets are integrated on the AtmosAir™ V-Series bottom cover to help keep the mattress in place during foot section extension / retraction.
Figure 5
Finished Installation
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Pump Installation 1.
Place pump on a horizontal surface or suspend on end of bed frame with built-in hanger.
2.
Attach pump hoses to mattress, as shown at right (Figure 6):
Figure 6
A Models (Alternating Pressure): • Attach blue hoses to the mattress connectors on the patient left side (marked with BLUE tag) of the mattress for alternating pressure. AR Models (alternating pressure / rotation): • Attach blue hoses to the mattress connectors on the patient left side (marked with BLUE tag) of the mattress for alternating pressure.
Tag Mattress Connectors
Pump Hoses
• Attach red hoses to the mattress connectors on the patient right side (marked with RED tag) of the mattress for rotation. 3.
Ensure air hoses are not kinked and will not be pinched by any articulated bed mechanisms.
4.
Plug pump unit into a properly-grounded wall outlet.
5.
Verify power to this outlet is not controlled by a wall switch.
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Patient Placement and Nursing Care It is recommended that all sections of this guide be read prior to product use. Carefully review the Contraindications, Safety Information, and Risks and Precautions sections prior to placing a patient on any AtmosAir™ MRS. 1.
Transfer patient following all applicable safety rules and institution protocols.
2.
Center patient side-to-side and head-to-foot on AtmosAir™ MRS surface.
Alternating Pressure / Rotation Adjustment The AtmosAir™ with SAT™ 9000, APod™ 25, and T-Series A and AR models provide alternating pressure and / or rotation. The level of alternating pressure or rotation can be adjusted for patient comfort. Prior to engaging alternating pressure or rotation, ensure that bed frame has side rails and that all side rails are fully engaged in full upright and locked position.
Ensure pump hoses are properly connected to appropriate side of mattress for the desired function (see Pump Installation). • Rotate the control knob on the pump clockwise to increase the intensity of alternating pressure relief or the level of rotation. • Rotate the control knob on the pump counter-clockwise to reduce the intensity of alternating pressure relief or the level of rotation. The AtmosAir™ MRS DOES NOT provide a Nurse Hold function.
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MAX.
MIN.
ALT. PRESSURE / ROTATION
CPR 1.
Level bed.
2.
Disconnect hoses from pump to level mattress (for A and AR models), as shown at right.
3.
Lower or remove side rail on caregiver’s side if necessary.
4.
Begin CPR.
5.
After CPR is performed:
Figure 7
• Reconnect pump hoses to mattress (for A and AR models). • Raise or install side rail as necessary. • Reconfigure bed and accessories as in initial placement.
Skin Care • Remove excess moisture and keep skin dry and clean. • Check patient’s skin regularly, particularly in areas where incontinence and drainage occur. • Ensure linens under patient are not wrinkled.
Incontinence / Drainage • Use moisture-impermeable underpads for incontinent patients. • Wipe surface clean and replace bed linens as required (see Care and Cleaning for cleaning instructions, if needed).
General Operation Avoid contact of sharp instruments with the AtmosAir™ MRS. Punctures, cuts and tears may prevent proper inflation and air pressure maintenance.
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Care and Cleaning General Instructions • Do not clean with solvents or alcohol. Solvent Alcohol • Do not launder (machine-wash) any AtmosAir™ MRS surface or mattress components. • For regular cleaning, use a mild detergent with water on a non-abrasive cloth. SOAP • To disinfect, use only EPA-approved disinfectants diluted in accordance with manufacturer’s instructions. • When blood and / or body fluids are present, use the following throughout all cleaning procedures: • Disposable, powder-free latex or latex-free gloves. • Protective clothing, including disposable or reusable impervious apron or gown. • Protective eyewear and face shield, as necessary.
Cleaning Mattress During Single Patient Use The AtmosAir™ MRS should be wiped daily with a mild soap and water solution. Always use standard precautions, treating all used equipment as contaminated. Institutions should follow local protocols for cleaning and disinfection. 1.
Unplug pump (for A and AR models) before cleaning.
2.
Remove or push bed linens to center of mattress.
3.
Wipe and rinse any soiling from the mattress surface.
4.
Dry surface with towel.
5.
Ensure bed linens are refitted and not wrinkled under patient.
6.
Clean pump and tubes (if needed) by wiping with a damp cloth.
Cleaning Mattress Between Multiple Patient Uses The AtmosAir™ MRS must be disinfected after each patient use. Always use standard precautions, treating all used equipment as contaminated. Institutions should follow local protocols for cleaning and disinfection.
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1.
Clean entire mattress surface with a coarse cloth using an EPA-approved disinfectant mixed to manufacturer’s instructions.
2.
Follow manufacturer recommendations regarding disinfectant application and contact time.
3.
Disinfect clean surface with a chlorine solution mixed to proper concentration, 1:100 (two ounces of chlorine bleach to one gallon of water.) Using a clean cloth, wring out excess chlorine solution until cloth is damp. Wipe entire surface with damp cloth.
4.
Allow to air dry.
Cleaning Air Pump and Tubes (A and AR models) 1.
Ensure pump is unplugged.
2.
Wipe surface of pump and tubes with coarse cloth using an EPA-approved disinfectant germicide mixed to manufacturer’s instructions. Do not flood any part of the pump with cleaning solution. Avoid spilling fluids on pump controls. If spills do occur, clean fluid from pump wearing rubber gloves or while unit is unplugged to avoid any possibility of shock. Once fluid is removed, check operation of components in area of spill. Fluids remaining on controls can cause corrosion, which may cause components to fail or operate erratically, possibly producing potential hazards for patient and staff.
3.
Wipe off excess solution.
4.
Disinfect pump and tubes a with chlorine solution (mixed according to the instructions in Cleaning Mattress Between Multiple Patient Uses). Using a clean cloth, wring out excess solution until cloth is damp. Wipe pump surface and tubes with damp cloth.
5.
Allow to air dry.
Preventive Maintenance Schedule Preventive maintenance for the AtmosAir™ MRS consists of regular cleaning (see Care and Cleaning) and an overall system check-out to be performed at the intervals described below. All components must be cleaned, disinfected and inspected after each patient’s use and before use by a new patient. Always use standard precautions, treating all used equipment as contaminated. Institutions should follow local protocols for cleaning and disinfection.
Daily Cleaning The cover should be wiped daily with a mild soap and water solution.
Weekly Cleaning The pump and hoses of A and AR models should be cleaned weekly.
Inspection / System Check-Out Check each of the following before placing the AtmosAir™ MRS with a new patient: 1.
Check mattress surface for tears or cracking; do not use if tears or cracks are present.
2.
Ensure mattress is free of stains and is not overly faded.
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For A and AR models: 1.
Ensure air inlet hoses and connectors on mattress and pump are clean and undamaged.
2.
Ensure pump and power cord are clean and undamaged.
3.
Ensure pump hanger brackets are secure and operate correctly.
4.
Ensure OFF / ON power switch and comfort control knob both operate correctly.
5.
Attach pump to the red rotation hoses and power up to ensure that the mattress surface tilts and there are no air leaks.
6.
Attach pump to the blue alternating pressure hoses and power up to ensure there are no air leaks.
Troubleshooting It is recommended that all sections of this guide be reviewed before troubleshooting any AtmosAir™ Mattress Replacement System. Do not attempt troubleshooting outside this guide or where the remedy recommends to contact a KCI service representative. Any unauthorized service, modification, alteration, or misuse may lead to serious injury and / or product damage and will void all applicable warranties. SYMPTOM
POSSIBLE CAUSE
SOLUTION
Green lamp on pump does not light when power switch is set to the ON position.
Power cord may be unplugged.
Plug in power cord.
Wall outlet may be controlled by a wall switch.
Plug power cord into different wall outlet.
Circuit breaker for wall switch may be tripped or blown.
Reset circuit breaker or replace fuse.
Power cord or power switch may be damaged.
Contact KCI customer service for assistance.
Tubing not connected properly.
Ensure red hoses are connected to hoses marked with red tag for rotation.
Tubing kinked.
Check tubing inside mattress for kinks.
Tubing disconnected.
Check tubing inside mattress for possible disconnect.
Mattress inflates only to one side when in rotation mode.
Hole in rotation bladder.
Check deflated rotation bladder for holes.
Mattress too firm upon arrival.
Difference in altitude not sufficient to open valves.
Apply weight to mattress to open valves.
Mattress cover too wrinkled upon removal from shipping container.
Internal components have not accomodated to environment. (This does not affect inflation or function).
Let mattress accommodate for 24 hours. If problem continues, contact KCI customer service for assistance.
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Parts Diagram - AtmosAir™ with SAT™ 4000 All hoses were removed to improve diagram readability. The optional fire barrier is a sleeve that fits over the foam and SAT™ assemblies. The SAT™ Cover, SAT™ Cells, SAT™ Interliner and rotation bladders (for A and AR models) are all part of the integrated SAT™ System and cannot be ordered separately. See Replacement Parts for a complete list of SAT™ Systems.
Mattress Cover Foam
SAT Cover (part of SAT System)
SAT Interliner (part of SAT System)
SAT Cell (part of SAT System)
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Parts Diagram - AtmosAir™ with SAT™ 9000, T-Series and V-Series All hoses were removed to improve diagram readability. The optional Fire Barrier is a sleeve that fits over the foam and SAT™ assemblies. The SAT™ Cover, SAT™ Cells, SAT™ Interliner and rotation bladders (for A and AR models) are all part of the integrated SAT System and cannot be ordered separately. See Replacement Parts for a complete list of SAT™ Systems.
Mattress Cover Foam
SAT Cover (part of SAT System)
Rotation Bladders (A and AR models only) SAT Interliner (part of SAT System)
SAT Cell* (part of SAT System)
*9000 Series and T-Series contain nine SAT cells, V-Series contains eight SAT cells.
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Parts Diagram - AtmosAir™ APod™ 25 Series All hoses were removed to improve diagram readability. The optional Fire Barrier is a sleeve that fits over the foam and SAT™ assemblies. The SAT™ Cover, SAT™ Cells, SAT™ Interliner, SAT™ Air Pods and rotation bladders (for A and AR models) are all part of the integrated SAT™ System and cannot be ordered separately. See Replacement Parts for a complete list of SAT™ Systems.
Mattress Cover Foam
SAT Cover (part of SAT System) SAT Air Pod (part of SAT System) Rotation Bladders (A and AR models only)
SAT Interliner (part of SAT System)
SAT Cell* (part of SAT System)
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Parts Diagram - AtmosAir™ Pump (A and AR models) See Replacement Parts for a complete list of parts that may be ordered for the AtmosAir™ Pump, as well as entire pump systems.
Pump Filter Cap
Pump Filter
Pump Unit
Harness / Tubing Connector Assembley
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Replacement Parts Do not attempt troubleshooting, maintenance, or parts replacement outside this manual or where the remedy recommends contacting a KCI service representative. Any unauthorized service, modification, alteration or misuse may lead to serious injury and / or product damage and will void all applicable warranties. Replaceable AtmosAir™ components are listed below. For more information such as pricing or additional spare parts that are not on this list, please contact your local KCI sales representative or contact KCI at 1-800-275-4524 for additional assistance.
ATMOSAIR™ MATTRESS COMPONENTS AtmosAir™ Foam Shells PART TYPE ... CATALOG NUMBER 4000/9000 Foam Shell ...KA4/9-FS(SIZE) APod™ 25 Foam Shell ...25P-FS(SIZE) T-Series Foam Shell... KT-FS3584 V-Series Foam Shell ... KV-FS3584 AtmosAir™ with SAT™ System PART TYPE ... CATALOG NUMBER 4000 SAT™ System (Fits mattresses 32-37 in wide) ...KA4-SAT 9000 SAT™ System (Fits mattresses 32-37 in wide), compatible with T-Series Mattress ...KA9-SAT 9000A SAT™ System (Fits mattresses 32-37 in wide), compatible with T-Series A Mattress ... KA9A-SAT 9000AR SAT™ System (Fits mattresses 32-37 in wide), compatible with T-Series AR Mattress ... KA9AR-SAT APod™ 25 SAT™ (Fits mattresses 32-37 in wide) ... 25P-SAT APod™ 25A SAT™ (Fits mattresses 32-37 in wide) ... 25PA-SAT APod™ 25AR SAT™ (Fits mattresses 32-37 in wide) ... 25PAR-SAT V-Series SAT™ System ... KV-SAT AtmosAir™ Fire Sleeve (Optional on all models except AtmosAir™ V-Series) PART TYPE ... CATALOG NUMBER AtmosAir™ Fire Barrier Lining... 407013 AtmosAir™ Side Bolster (Optional on 4000, 9000 and APod™ 25 models including A and AR versions) PART TYPE ... CATALOG NUMBER AtmosAir™ Raised Side Bolster... 407012 Integrated side bolster built into foam shell to keep patients centered, must be ordered with foam shell at point of purchase.
ATMOSAIR™ MATTRESS COVERS AtmosAir™ Model 4000 Mattress PART TYPE ... CATALOG NUMBER Top Cover Only, TheraTex™ ... KA4C-SO(SIZE) Top Cover Only, Multi-Stretch... KA4C-RE(SIZE) Top Cover Only, Anti-Shear ... KA4C-RP(SIZE) Bottom Cover Only, Non-Skid... KA4C-NB(SIZE) Bottom Cover Only, Vinyl Gray ... KA4C-VG(SIZE) 17
AtmosAir™ Model 9000 Mattress PART TYPE ... CATALOG NUMBER Top Cover Only, TheraTex™ ... KA9C-SO(SIZE) Top Cover Only, Multi-Stretch... KA9C-RE(SIZE) Top Cover Only, Anti-Shear ... KA9C-RP(SIZE) Bottom Cover Only, Non-Skid... KA9C-NB(SIZE) Bottom Cover Only, Vinyl Gray ... KA9C-VG(SIZE) AtmosAir™ Model 9000A Mattress with Alternating Pressure PART TYPE ... CATALOG NUMBER Top Cover Only, TheraTex™ ... KA9CA-SO(SIZE) Top Cover Only, Multi-Stretch...KA9CA-RE(SIZE) Top Cover Only, Anti-Shear ...KA9CA-RP(SIZE) Bottom Cover Only, Non-Skid... KA9CA-NB(SIZE) Bottom Cover Only, Vinyl Gray ...KA9CA-VG(SIZE) AtmosAir™ Model 9000A Mattress with Alternating Pressure PART TYPE ... CATALOG NUMBER Top Cover Only, TheraTex™ ... KA9CA-SO(SIZE) Top Cover Only, Multi-Stretch...KA9CA-RE(SIZE) Top Cover Only, Anti-Shear ...KA9CA-RP(SIZE) Bottom Cover Only, Non-Skid... KA9CA-NB(SIZE) Bottom Cover Only, Vinyl Gray ...KA9CA-VG(SIZE) AtmosAir™ Model 9000A Mattress with Alternating Pressure and Rotation PART TYPE ... CATALOG NUMBER Top Cover Only, TheraTex™ ... KA9CAR-SO(SIZE) Top Cover Only, Multi-Stretch...KA9CAR-RE(SIZE) Top Cover Only, Anti-Shear ...KA9CAR-RP(SIZE) Bottom Cover Only, Non-Skid... KA9CAR-NB(SIZE) Bottom Cover Only, Vinyl Gray ...KA9CAR-VG(SIZE) AtmosAir™ Model APod™ 25 Mattress PART TYPE ... CATALOG NUMBER Top Cover Only, TheraTex™ ... 25PC-SO(SIZE) Top Cover Only, Multi-Stretch...25PC-RE(SIZE) Top Cover Only, Anti-Shear ...25PC-RP(SIZE) Bottom Cover Only, Non-Skid... 25PC-NB(SIZE) Bottom Cover Only, Vinyl Gray ...25PC-VG(SIZE) AtmosAir™ Model APod™ 25 A Mattress with Alternating Pressure PART TYPE ... CATALOG NUMBER Top Cover Only, TheraTex™ ... 25PCAP-SO(SIZE) Top Cover Only, Multi-Stretch...25PCAP-RE(SIZE) Top Cover Only, Anti-Shear ...25PCAP-RP(SIZE) Bottom Cover Only, Non-Skid... 25PCAP-NB(SIZE) Bottom Cover Only, Vinyl Gray ...25PCAP-VG(SIZE)
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