Stryker Isolibrium PE Manuel D'utilisation page 8

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 Stryker Model 297300000000 I I s s o o l l i i b b r r i i u u m m PE is a powered support surface with features that provide pressure
redistribution, low air loss, turn assist, max inflate, and lateral rotation. The I I s s o o l l i i b b r r i i u u m m PE powered support surface is for
use with the Stryker Model 300900000000 P P r r o o C C u u i i t t y y ™ bed frame.
I I n n d d i i c c a a t t i i o o n n s s f f o o r r u u s s e e
The Stryker Model 297300000000 I I s s o o l l i i b b r r i i u u m m PE support surface is intended to assist in the prevention and treatment of all
pressure injury or pressure ulcers (includes all stages, unstageable and deep tissue pressure injury). As a
recommendation, healthcare professional should complete a clinical evaluation of risk factors and skin assessments. The
intended users is both healthcare HCPs (nurses, nurse aids, and medical doctors), transporters, and human patients. This
product is for use by human patients in a health delivery organization (HDO).
The I I s s o o l l i i b b r r i i u u m m PE patient-specific immersion is intended to assist in the management of microclimate of the patient's skin,
patient repositioning, and the support in prevention of early mobility and pulmonary complications.
The I I s s o o l l i i b b r r i i u u m m PE powered support surface is not intended for use in or with:
• Oxygen rich environments
• Sterile environments
• Home care or long-term care facility settings
• Behavioral health populations
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 o o n n t t r r a a i i n n d d i i c c a a t t i i o o n n s s
I I s s o o l l i i b b r r i i u u m m P P E E is contraindicated for use on patients with:
• Unstable fractures
• Unstable spinal cord injuries
EN 4 2973-009-005 Rev AF.0