• Provides sustained therapeutic compression for up to 7 days
• Clinically proven to significantly reduce slippage and improve patients' daily living activities
• Designed to be applied at full stretch, reducing application variability for consistent, reliable compression at every application
• Easy and fast to apply
• Thin, lightweight, breathable sleeve allows patients to wear their own shoes, so they can return to their regular daily activities
• Not made with natural rubber latex

3M™ Coban™ 2 Two-Layer Compression System is intended for the management of venous leg ulcers, lymphedema and other clinical conditions where compression is appropriate. 3M™ Coban™ 2 Two-Layer Compression System may be used for patients with an ABPI greater than or equal to 0.8. 3M™ Coban™ 2 Lite Two-Layer Compression System may be used for patients with an ABPI greater than or equal to 0.5.

Decompensated heart insufficiency NYHA Class IV, ACC/AHA Stage D 
Septic phlebitis 
Phlegmasia coerulea dolens and other conditions contraindicated according to established guidelines or local procedures
Known hypersensitivity to any of the component materials

Coban™ 2 Compression System: 
Severe arterial occlusive disease with an ABPI of less than 0.8

Coban™ 2 Lite Compression System: 
Severe arterial occlusive disease with an ABPI of less than 0.5

Coban™ 2 (Lite) Compression System should be used under the supervision of a licensed health care professional. Patients with known arterial insufficiency, decompensated heart insufficiency or diabetes with advanced small vessel disease may not tolerate compression.
Wrapping too tightly may impair circulation. Monitor the area of application frequently for signs of discoloration, pain, numbness, tingling or other changes in sensation and swelling. If these symptoms occur, patients should be advised to remove Coban™ 2 (Lite) Compression System and promptly contact their health care provider.
Patients new to compression therapy may not initially tolerate the pressure level provided. For these patients, the Compression Layer may be initially applied with less than full stretch or Coban™ 2 Lite Compression System can be used.
Coban™ 2 (Lite) Compression System is not designed as a wound dressing. Wounds should be managed with dressings appropriate to the wound condition.
Coban™ 2 (Lite) Compression System should be changed if it becomes loose fitting, or when it no longer conforms to the shape of the bandaged area. The patient should contact their health care professional to determine if it should be replaced.
Patients should be advised to keep Coban™ 2 (Lite) Compression System dry. If the bandage becomes wet, patients should contact their health care provider to determine if it should be replaced.
For thorax applications, Coban™ 2 Lite Compression System may be more comfortable for some patients.
Do not reuse. Reuse may result in compromising product integrity or lead to device failure.
At the discretion of the health care professional, patients or their care providers can be trained to apply the bandage for subsequent applications.

Store Coban™ 2 (Lite) Compression System in its individual package until use. Avoid excessive heat and humidity. For shelf life, refer to the date printed on the packaging (see explanation of symbols below).
Coban 2™ (Lite) Compression System can be disposed as normal hospital/household waste or according to facility procedures for waste handling