
Specifications
| Model | LI 1003 |
|---|---|
| Category | Liners and attachments |
| Material | High-strength medical silicone |
| Distal cushion | 14.3 mm for additional comfort |
| Outer cover | Fabric covering made of circular knit fabric for abrasion resistance |
| Color | Blue |
| Manufacturer | Orliman SLU, (Spain) |
Liners and attachments
Silicone liner ACTIVE fabric cover Orliman LI 1003
Model: LI 1003
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Product description
Made from high-strength medical silicone and featuring an outer fabric covering for long-lasting use. Silicone liner ACTIVE with fabric covering and distal attachment Orliman LI 1003 Silicone liners for lower leg amputation are made from high-strength medical silicone that is easy to clean. Thanks to available different material densities, the liners provide comfort and necessary support for patients with varying activity levels. The distal area of the liner has a 14.3 mm cushion for additional comfort and skin protection, helping to adapt to scar irregularities, reduce rotational moments, and impact loads during walking. FEATURES: Medical Silicone: Made from high-strength medical silicone, easy to clean and wear-resistant. Distal Cushion: A 14.3 mm thick cushion provides additional comfort and skin protection, especially in scar areas, helping to reduce rotational moments and distal impacts during loading. Outer Covering: The liner has an outer textile covering that provides high abrasion resistance and ensures a long service life by absorbing friction between the silicone and the rigid prosthesis base. Matrix: The liner features a 10 cm long matrix that stabilizes the limb's soft tissues, limiting their stretching and minimizing the "piston" effect during walking. LINER FUNCTIONS: Silicone tightly adheres to the skin, preventing irritation and friction. Improved blood circulation due to distal compression. Even pressure distribution on the limb surface. Skin protection from scars and irregularities. Reduction of the "piston" effect during walking. Orliman silicone liners comply with all requirements of EU Directive 93/42/CEE (RD. 1591/2009). All necessary tests were conducted in accordance with the European quality standard for prosthetic and orthopedic products (EN ISO 22523).