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DYNA-FLEX™ Multi-Layer Compression System


DYNA-FLEX™ Multi-Layer Compression System
DYNA-FLEX™ Multi-Layer Compression System
DYNA-FLEX™ Multi-Layer Compression System
DYNA-FLEX™ Multi-Layer Compression System

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.
 

Overview

Providing Comfort

First layer
The padding and absorption layer is soft, light and breathable.
• Helps protect the patient from pressure points
• Absorbent
• Comfortable for the patient

Easy Application

Second layer
The compression bandage uses an innovative, patented visual cue to aid proper application. The bandage is printed with a rectangular pattern that turns to a square when correct level of stretch is achieved. This assists in achieving reproducible pressures from one practitioner to another.

Providing Security

Third layer
The cohesive compression bandage helps prevent slippage and increases compliance.

System Components & Accessories

How it Works

  • About
  • Specifications
  • Materials For Download

About

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
 

Specifications

DYNA-FLEX™ Multi-Layer Compression System

Contents
1 ADAPTIC™ Non-Adhering Dressing (sterile)
5 in x 9 in (12.7 cm x 22.9 cm)
 
A primary dressing made of knitted cellulose acetate fabric and impregnated with a specially formulated petrolatum emulsion.
It is designed to help protect the wound while preventing the dressing from adhering to the wound.

1 DYNA-FLEX™ Compression System Layer One (Padding/Absorption Layer) (non-sterile)
4 in x 156 in (10.2 cm x 396.2 cm)

1 DYNA-FLEX™ Compression System Layer Two (Compression Bandage) (non-sterile)
4 in x 108 in (10.2 cm x 274.3 cm)

1 DYNA-FLEX™ Compression System Layer Three (Cohesive Compression Bandage) (non-sterile)
4 in x 98 in (10.2 cm x 248.9 cm)

CAUTION: THIS PRODUCT CONTAINS NATURAL RUBBER LATEX WHICH MAY CAUSE ALLERGIC REACTIONS.

Indications & Applications

Indications & Applications

  • Indications
  • Applications

Indications for Use

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.
 
Contra-indications
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.
 
 
Before use, physicians should review complete risk information and essential prescribing information which can be found in the Product Instructions for Use. To order any of the products listed below, please call 1-800-275-4524.
 

Applications

Application Instructions
1. Confirm the absence of arterial or diabetic small vessel disease. (Before first application.)
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 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.
5. DYNA-FLEX™ Compression System Layer Two (Compression Bandage, Green Labeled Bandage): To secure in place, wrap the compression bandage from the base of the toes to the ankle using the spiral technique. Begin using the figure eight technique at 50% extension from the ankle to just below the knee. Cut off any excess bandage to avoid overlap at the knee. To assist in wrapping it is recommended that the rectangular pattern on the bandage be
stretched to a square pattern. Secure end of Layer Two 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.
 
Caution: Federal Law (USA) restricts this device to sale by or on the order of a properly licensed healthcare practitioner.
¹in vitro data on file.
 

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

Clinical Evidence

Additional summary of evidence and outcomes.

Evidence & Outcomes

Evidence & Outcomes

Title Study Type Date Authors