IInnttrroodduuccttiioonn
This manual assists you with the operation or maintenance of your Stryker product. Read this manual before operating or
maintaining this product. Set methods and procedures to educate and train your staff on the safe operation or maintenance
of this product.
CCAAUUTTIIOONN
• Improper usage of the product can cause injury to the patient or operator. Operate the product only as described in this
manual.
• Do not modify the product or any components of the product. Modifying the product can cause unpredictable operation
resulting in injury to patient or operator. Modifying the product also voids its warranty.
NNoottee
• This manual is a permanent part of the product and should remain with the product even if the product is sold.
• Stryker continually seeks advancements in product design and quality. This manual contains the most current product
information available at the time of printing. There may be minor discrepancies between your product and this manual. If
you have any questions, contact Stryker Customer Service or Technical Support at 1-800-327-0770.
PPrroodduucctt ddeessccrriippttiioonn
IIssoolliibbrriiuumm®, Stryker Model 2971/2972, is a powered support surface with features that provide Pressure Redistribution,
Low Air Loss, and Lateral Rotation. IIssoolliibbrriiuumm is for use with the IInnTToouucchh®® (revisions 4.0 or higher software) bed frame.
IIssoolliibbrriiuumm and IInnTToouucchh are an integrated bed and surface system that caregivers use to assist in patient care.
IInntteennddeedd uussee
The IIssoolliibbrriiuumm support surface assists in the prevention and treatment of all pressure injury stages (including stages 1, 2,
3, 4, Unstageable and Deep Tissue Pressure Injury). Before implementing IIssoolliibbrriiuumm, a healthcare professional should
complete a clinical evaluation of risk factors and skin assessments. The IIssoolliibbrriiuumm patient-specific immersion to assist in
managing microclimate of the patient skin, patient repositioning, early mobility, and the prevention of pulmonary
complications.
The IInnTToouucchh and IIssoolliibbrriiuumm system is for use by patients in an acute care setting. The acute care settings may include
critical care, step down, progressive care, medical / surgical, sub-acute care, and post anesthesia care unit (PACU), or
other locations as prescribed. The patient, accessories, and any extra loading must not exceed the safe working load of
IInnTToouucchh or IIssoolliibbrriiuumm.
The operators for the system are healthcare professionals (nurses, nurse aids, and doctors) who can use all system
operations (for example: bed motion functions, nurse call, siderail communications, bed exit, or therapy options). Patients
and bystanders can use the bed motion functions, nurse call, and siderail communications but are restricted from the use of
the powered support surface functions. Trained professionals install, service, and calibrate the IInnTToouucchh and IIssoolliibbrriiuumm
system.
EExxppeecctteedd sseerrvviiccee lliiffee
IIssoolliibbrriiuumm support surface has a five year expected service life under normal use, conditions, and with appropriate periodic
maintenance.
IIssoolliibbrriiuumm covers (top and bottom) have a two year expected service life under normal use, and conditions.
CCoonnttrraaiinnddiiccaattiioonnss
Stryker promotes the clinical assessment of each patient and appropriate usage by the operator.
2971-009-002 Rev D.0 3 EN
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