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Stryker IsoTour 2872 Manual De Operaciones página 8

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I I n n t t r r o o d d u u c c t t i i o o n n
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.
C C A A U U T T I I O O N N
• 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.
N N o o t t e e
• 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.
P P r r o o d d u u c c t t d d e e s s c c r r i i p p t t i i o o n n
The S S t t r r y y k k e e r r Model 2872, I I s s o o T T o o u u r r support surface is a non-powered or powered gel-filled support surface. This product
was designed to help manage shear and provide pressure redistribution aided by the T T r r u u T T u u r r n n ™ ™ feature. The cover helps
manage microclimate. I I s s o o T T o o u u r r shall be used with a support surface cover at all times. This product is for use on acute care
hospital bed frames.
I I n n t t e e n n d d e e d d u u s s e e
The I I s s o o T T o o u u r r support surface assists in the prevention and treatment of pressure injuries or pressure ulcers (all stages,
Unstageable injury, and Deep Tissue injury). We recommend you implement this product in combination with clinical
evaluation of risk factors and skin assessments made by a healthcare professional.
This support surface is for use with human patients with existing or at risk of incurring pressure injuries. The patient must
not exceed the safe working load as noted in the specification section of this manual.
This support surface is for use by patients in an acute care setting. This may include critical care, step down, progressive
care, med/surg, sub-acute care, and post anesthesia care unit (PACU), or other locations as prescribed by a physician.
Operators of this support surface include healthcare professionals (such as nurses, nurse aids, or doctors).
This product is not intended to be sterile, include a measuring function, or used in a home healthcare environment.
C C l l i i n n i i c c a a l l b b e e n n e e f f i i t t s s
Assists in the prevention and treatment of all pressure ulcers or pressure injuries
C C l l i i n n i i c c a a l l a a s s s s e e s s s s m m e e n n t t
The T T r r u u T T u u r r n n feature is for use only after you complete a clinical assessment per your hospital protocol. This is to make
sure that no adverse reaction would result for patients with the following example conditions:
Spinal cord injury, except for unstable spine, see Contraindications
Skeletal traction
Significant hemoptysis
Bleeding disorders
EN
4
2872-009-005 Rev B.1

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