Description
Biflex Self-Adjust Arm is an adjustable compression device designed to provide effective support for managing venous and lymphatic conditions. It ensures consistent pressure, is easy to apply, and enhances comfort with its breathable, latex-free material.
The design of Biflex Self Adjust Arm focuses on user comfort and convenience. The overlapping strap design ensures comprehensive coverage of the limb, preventing the migration of oedema and providing uniform compression across the arm. This feature is crucial in maintaining effective therapy and ensuring that the compression is evenly distributed, thereby enhancing the therapeutic benefits.
The stretchable inner loop acts as a “third hand”, assisting users in donning and doffing the garment easily. This feature is particularly beneficial for individuals who may have limited dexterity or strength, ensuring that the garment can be applied without additional help.
Biflex Self Adjust Arm is made from breathable, high-quality materials that ensure comfort during prolonged use. The materials are also latex-free, reducing the risk of allergic reactions.
– Adjustable compression: adjustable, short-stretch, inelastic compression system.
– Full limb coverage: overlapped bandages design and reversed closures for a complete covering of the limb to avoid oedema migration.
– Comfortable: breathable, thanks to open cell foam.
– Easier movement: the product is removable at the elbow to facilitate patient movement.
– Easy to set up: easy donning and doffing thanks to a stretchable inner loop acting as a “third hand”.
– Color: beige color.
– Latex free.
Indications
- Oedema management (venous, lymphatic and traumatic origin)
- Chronic venous insufficiency
- Supportive care of lipoedema
Essential Information
Biflex Self Adjust Arm is designed to be worn in conjunction with Biflex Self Adjust Hand as appropriate for your individual compression need.
If you are new to wearing compression therapy, changing the type or Class of your garment or have any existing medical conditions we advise that you are assessed and measured by a suitably trained healthcare professional.
The medical device class I, mentioned on this document is CE marked according to the European Regulation 2017/745 on medical devices.
Please read carefully the instructions for use of the product.