View Abstract on PubMed
The Comfortable and Easy to Apply Compression System
DYNA-FLEX™ Multi-Layer Compression System is a multi-layer system that provides proven and sustained compression1- supporting compression therapy for venous insufficiency.2
1st layer: This padding and absorption layer is soft, light, and breathable.
2nd layer: This compression bandage uses an innovative, patented visual cue to aid proper application: a rectangular pattern that turns square when the correct level of stretch is achieved. This assists healthcare practitioners in achieving consistent, reproducible pressure.
3rd layer: This cohesive compression bandage helps prevent slippage, while increasing compliance.
To order any of the products listed below, please contact your KCI representative or call your local KCI Office. Click here to contact us.
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Overview
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How it Works
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Indications & Applications
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Evidence & Outcomes
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Ordering
Overview

• Helps protect the patient from pressure points
• Absorbent
• Comfortable for the patient


The cohesive compression bandage helps prevent slippage and increases compliance.
How it Works
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ABOUT
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SPECIFICATIONS
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MATERIALS FOR DOWNLOAD
DYNA-FLEX™ Multi-Layer Compression System is suitable for use on patients requiring compression bandage management of the lower leg, with an ankle circumference 18 cm or larger (padded).
The DYNA-FLEX™ Compression System kit consists of 3 layers, also included is ADAPTIC™ Non-Adhering Dressing. When used according to package insert directions, this Multi-Layer Compression System provides sustained compression for up to seven days at both the ankle and below the knee.
A kit contains:
- Layer 1: Blue labeled bandage
- Layer 2: Green labeled bandage
- Layer 3: Red labeled bandage
- ADAPTIC™ Non-Adhering Dressing
1 ADAPTIC™ Non-Adhering Dressing (sterile)
5 in x 9 in (12.7 cm x 22.9 cm)
4 in x 156 in (10.2 cm x 396.2 cm)
4 in x 108 in (10.2 cm x 274.3 cm)
4 in x 98 in (10.2 cm x 248.9 cm)
Indications & Applications
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INDICATIONS
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APPLICATIONS
DYNA-FLEX™ Compression System is indicated for the management of venous leg ulcers and related conditions. The compression system may be used on patients with an ankle circumference 18 cm or larger (padded). Compression data indicates that the DYNA-FLEX™ Compression System provides sustained compression for up to seven days at both the ankle and below the knee, when used according to package insert directions.
The DYNA-FLEX™ Compression System should not be used on diabetic patients with small vessel disease, patients with lymphedema as a result of cancer, or on patients with an ankle brachial index (ABI) of less than 0.8. Doppler ultrasound is recommended to rule out arterial disease.
If during use of this product, it becomes wet, slips, gaps, or becomes uncomfortable, creates irritation or you observe uncharacteristic color or odor from your foot, consult your clinician immediately.
Instructions for Use
Clinical Solutions for
2. Confirm ankle circumference is greater than 18 cm. (Ankle circumference may change as edema is reduced.)
3. Wound contact dressing: Carefully clean the wound following facility protocol and ensure skin surrounding the wound is dry. Cover the wound with ADAPTIC™ Non-Adhering Dressing. NOTE: DYNA-FLEX™ Multi-Layer Compression System may also be used over TIELLE™ Hydropolymer Foam Dressing, PROMOGRAN™ Matrix Wound Dressing or PROMOGRAN PRISMA™ Matrix.
4. DYNA-FLEX™ Compression System Layer One (Padding/Absorption Layer, Blue Labeled Bandage): To secure in place, wrap the padding/absorption layer against the skin. Use a spiral technique at 50% overlap from the base of the toes to just below the knee. Stretch this layer around bony prominence, such as the heel, to increase conformability. Cut off any excess bandage to avoid overlap at the knee. Secure end of Layer One with appropriate tape.
6. DYNA-FLEX™ Compression System Layer Three (Cohesive Compression Bandage, Red Labeled Bandage): Wrap the cohesive compression bandage from the base of the toes to just below the knee using the spiral technique at 50% extension and 50% overlap. Cut off any excess bandage to avoid overlap at the knee.
7. Removal: DYNA-FLEX™ Compression System should be removed by a clinician with blunt scissors. After removal, clean and assess wound, chart progress, and continue treatment as necessary. Dispose of the contaminated dressing and wraps using the resealable ziplock package provided with the system.
Instructions for Use
Clinical Solutions for
Evidence & Outcomes
Acelity Clinical Evidence is a resource for healthcare professionals to explore preclinical, clinical, and review articles discussing the use of KCI and Systagenix products. Use our powerful search tool to customize your view of the Acelity product evidence.
For questions or to request published literature contact Medical Information
TITLE | STUDY TYPE | DATE | AUTHORS |
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Using ACTISORB™: Case Studies International case series |
International case series | 2012 | London: Wounds International. |
View Abstract on PubMed
Ordering
To order any of the products listed below, please contact your KCI representative or call your local KCI Office. Click here to contact us.
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DYNA-FLEX™ Compression System
PRODUCT PRODUCT CODE ORDERING OPTION DYNA-FLEX™ Multi-Layer Compression System
3 Bandages and (1) 5" X 9" ADAPTIC™ Non-Adhering Dressing
7025 8 units/case/7025
A6223 - ADAPTIC™ Non-Adhering Dressing
A6421 - 1st Layer
A6430 - 2nd Layer
A6438 - 3rd Layer