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McKesson Non-Sterile Four-Layer Compression Bandage System

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McKesson Non-Sterile Four-Layer Compression Bandage System is a superior bandaging system for optimum compression and absorbency in the management of venous leg ulcers and related conditions. It is composed of four bandages that work together, providing effective sustained compression for up to seven days when applied as directed. It is not made of natural rubber latex.

McKesson Compression Bandage System Highlights

  • Layer One, a non-woven padding
  • Layer Two is a crepe bandage
  • Layer Three is a light compression bandage
  • Layer Four is a cohesive bandage

McKesson Four-Layer Compression Bandage System Features

  • McKesson Non-Sterile Four-Layer Compression Bandage System bandage dimensions:
    - Padding Bandage: 4" x 3.8 yds. (10 cm x 3.5 m) unstretched
    - Crepe Bandage: 4" x 4.9 yds. (10 cm x 4.5 m) stretched
    - Compression Bandage: 4" x 9.5 yds. (10 cm x 8.7 m) stretched
    - Cohesive Bandage: 4" x 6.5 yds. (10 cm x 6.0 m) stretched
  • Layer 1: A non-woven padding, is composed of a blend of synthetic materials that absorbs wound exudate. This highly comfortable layer primarily provides protection to bony prominences
  • Layer 2: A crepe bandage which anchors and smoothes the padding layer while absorbing exudate
  • Layer 3: A light compression bandage that conforms to any contour while providing about one-half the compression of the system
  • Layer 4: A cohesive bandage that sticks to itself and secures the bandages without tape for week-long compression
  • Closure Type: Self-Adherent

When to Use Four-Layer Compression Bandage System?

  • Manage venous leg ulcers and related conditions. 
  • This system consists of four bandages that, when applied correctly, provide compression for seven days. 
  • Multi-layered system simultaneously absorbs, protects, and provides graduated sustained compression


Contraindications

  • Determine the Ankle Brachial Pressure Index (ABI) using a Doppler ultrasound.
  • An ABI less than 0.8 may indicate the presence of significant arterial disease.
  • Do not use this Bandaging System if the patient’s ABI is less than 0.8 or if arterial disease is suspected.
  • While using this product, if the patient develops pain, numbness, color changes, cool toes or foot, the patient should seek immediate medical attention.
  • Do not use this Bandaging System on patients with an ankle circumference less than 18 cm.
  • Apply extra padding as needed over boney prominences of the ankle and/or tibia to avoid pressure necrosis.


Change Frequency

  • Change dressing as directed by a healthcare professional







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