Summary of Contents for Span-America PressureGuard APM2
- Page 1 OWNER’S MANUAL PressureGuard APM2 ® Safety Supreme PressureGuard APM2 ® Span-America Medical Systems, Inc. Greenville, SC 29615 800-888-6752 P10331...
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Page 3: Table Of Contents
TABLE OF CONTENTS DOCUMENT SYMBOLS ..............................1 INTRODUCTION ................................2 DESCRIPTION INDICATIONS FOR USE MODES OF OPERATION CONSTRUCTION AND DESIGN FEATURES......................4 CONSTRUCTION AND DESIGN FEATURES DESCRIPTIONS ................. 5 DIRECTIONS FOR SET-UP ............................6 CONTROL UNIT FUNCTIONS ............................ 8 ELECTROMAGNETIC OR OTHER INTERFERENCE ..................10 POWER LOSS / PATIENT TRANSPORT ...................... - Page 4 P10331...
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Page 5: Document Symbols
Document Symbols This manual contains different typefaces and symbols to make the content easier to read and understand: Standard text – used for regular information. Boldface text – stresses a word or phrase. NOTE: - sets apart special information or important instruction clarification. ... -
Page 6: Introduction
INTRODUCTION PRESSUREGUARD APM2 SERIES Air therapy support surface DESCRIPTION: The system consists of a foam shell with a high-density foam topper serving as the support surface underneath the patient. The foam shell also includes Safety Edge bolsters at the sides of the mattress, providing added patient stability and positioning. - Page 7 Never operate this product if it has a damaged cord or plug, if it is not working properly, if it has been dropped or damaged, or dropped into water. Return the unit to Span-America Medical Systems, Inc. for examination and repair. Keep the cord away from heated surfaces. Discontinue use if power cord is damaged or worn.
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Page 8: Construction And Design Features
Shear Transfer Zones™ design (standard APM2 model only) (U.S. Patent # 8,438,682) In addition to the Geo-Matt® segmented top surface, Span-America’s exclusive Shear Transfer Zones™ design provides an additional measure of shearing protection in the form of the silicone-coated, shear-minimizing fabric bands located on the underside of the bi-directional stretch cover. -
Page 9: Construction And Design Features Descriptions
Construction and Design Features Illustration Descriptions The air-cylinder inflation system and the foam shell work in concert to maintain low interface pressures throughout the surface, making the mattress effective for prevention and treatment of pressure ulcers. [Illustration item ①] Both models include replaceable, zippered covers made with fabrics that are anti-microbial, flame-resistant, fluid-impervious, tear-resistant, and have a Covers: low moisture vapor transmission rate (MVTR). -
Page 10: Directions For Set-Up
DIRECTIONS FOR SET-UP 1. Place the PressureGuard mattress on the bed frame with the airline connectors at ® the foot end of the bed. The mattress has a gray vinyl side that should be down on the bed frame, and a green or silver fabric side that should be face up toward the patient. In-home models, (available for standard APM2 models only) have a dark blue fabric that should be face up toward the patient. - Page 11 Figure E Figure F Figure G 4. Ensure that the Toggle switch is in the “Alternating Pressure” position. 5. Ensure that green On/Off switch at side of control unit is “Off”. Plug power cord into wall outlet. Press On/Off switch “ON”. Never thread airline through mechanical parts of the bed or bed rails where normal bed movement may damage the airlines, power cord or the control unit itself.
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Page 12: Control Unit Functions
5900 Control Unit Functions Comfort Level Selection: Allows selection of air cylinder firmness within a relatively small range. Press “Softer” or “Firmer” button to achieve desired setting. Begin in softest setting, then adjust for comfort as desired. Mode Selection: Press button to select “Alternate”, “Float”, or “Auto Firm”. “Alternate”... - Page 13 5900 Control Unit Functions Continued “Float” (powered flotation therapy) mode: Suspends cyclical inflation/deflation of the air cylinders and instead provides powered flotation therapy. In this mode, all four air cylinders are evenly inflated, and the system maintains ideal pressure management by adjusting in response to any repositioning of the user on the surface.
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Page 14: Electromagnetic Or Other Interference
ELECTROMAGNETIC OR OTHER INTERFERENCE – see Appendix on page 20. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to other devices in the vicinity. However, there is no guarantee that interference will not occur in a particular installation. -
Page 15: Troubleshooting Patient Complaints
Do not use the mattress if the cover is damaged. BED RAILS: Due to concerns over the possibility of patient entrapment, Span-America recognizes that the use of rails of any length is a matter currently addressed by federal and state laws/guidelines, and by individual facility protocol. -
Page 16: Storage And Transportation
STORAGE AND TRANSPORTATION: Store the mattresses in a clean, dry place. Once the mattress is removed from the box, store in a flat position if possible. If mattress must be stored on its side, ensure that the inflation system is in correct position within the mattress prior to placing a user on the surface. - Page 17 For long-term incontinent applications, clean and disinfect cover daily. A scented cleaner/disinfectant is recommended. Iodophor type disinfectants (e.g. Betadine) will stain the fabric. For disinfection, phenolic or quaternary type disinfectants are recommended. Disinfectants should be hospital grade (tuberculocidal). Follow manufacturer’s instructions for use concentrations, contact times and rinsing.
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Page 18: Service
6. Inspect the cover of the control panel to assure that the covering is not cracked or damaged, allowing liquids or other conductive material to penetrate to the switches. 7. Report any unusual sounds, burning odors, or anything unusual to maintenance personnel. Discontinue use of the power cord immediately and contact Span-America Medical Systems, Inc. for replacement. Mattress Inspect the covers and zipper area for signs of damage, puncture, or wear that could result in fluid pass-through. -
Page 19: Specifications
SPECIFICATIONS Cover: Bacteriostatic, flame resistant, fluid-proof, tear resistant Foam: High-density open-cell polyurethane. Conforms to NFPA 101 small scale and Cal TB# 117. Air cylinders: Urethane Electrical: All control units 120 V, 60 H. With respect to electric shock, fire and mechanical hazards only in accordance with UL 60601-1. - Page 20 Flammability: All models comply with 2000 NFPA 101 (Life Safety Code), Cal. TB # 129 and 16 CFR 1632 and 1633. Parts: Replacement P10062 Replacement airline assembly with quick disconnect and transport lid P10049 replacement quick disconnect with transport lid P10063 Replacement airline only (without quick disconnect or transport lid) P10065...
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Page 21: Trouble Shooting Guide
Adjust each as necessary to meet patient needs while maximizing turn angle. Defective Control Unit Call for Service. Call Span-America for assistance Patient exceeds weight limit. with product selection. Control Unit is not turned on. Turn control unit on. - Page 22 Problem Possible Cause Solution Disconnect and reconnect airlines Low pressure indicator Airlines not connected. to verify they have all locked into illuminated. place. Airlines or quick disconnect Call for replacement. connectors are damaged. Defective Control Unit. Call for service. Call for replacement. To replace, turn mattress upside down and unzip cover.
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Page 23: Technical Description
TECHNICAL DESCRIPTION Item Specification Power Supply (Note: See rating AC 100-120V 60 Hz, 0.17A (for 120V system) label on the product) AC 220-240V 50 Hz, 0.07A (for 230V system) Fuse Rating T1A, 250V Cycle time Fixed Operation:10° C to 40° C (50° F to 104° F) Temperature Storage: -15°... -
Page 24: Appedix A: Emc Information
APPENDIX A: EMC INFORMATION Guidance and Manufacturer’s Declaration- Electromagnetic Emissions: This device is intended for use in the electromagnetic environment specified below. The user of this device should make sure it is used in such an environment. Emissions Test Compliance Electromagnetic Environment-Guidance The device uses RF energy only for its internal function. - Page 25 Guidance and Manufacturer’s Declaration - Electromagnetic Immunity: This device is intended for use in the electromagnetic environment specified below. The user of this device should make sure it is used in such an environment. Immunity Test IEC60601 test level Compliance Electromagnetic Environment-Guidance Portable and mobile RF communications equipment should be used no closer to any part of this device, including cables, than there commended...
- Page 26 Recommended separation distances between portable and mobile RF communications equipment and this device: This device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of this device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and this device as recommended below, according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter m...
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Page 27: Preventive Maintenance And Repair Log
PressureGuard APM2 Series Preventive Maintenance and Repair Log Date Air Filter Power Cord Mattress Repair Manufacturer: Span-America Serial #: C=Cleaned Date Purchased: OK=Okay R=Repaired/Replaced... - Page 30 THIS PRODUCT IS PROTECTED BY ONE OR MORE OF THE FOLLOWING U.S. PATENTS: 6,223,369 6,848,138, 8,438,682 SPAN-AMERICA MEDICAL SYSTEMS, INC. GREENVILLE, SC 800-888-6752 P10331...
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