Polymeric Mesh Endoprostheses “Lintex” for Reconstructive Surgery — Sterile

Polymeric Mesh Endoprostheses “Lintex” for Reconstructive Surgery — Sterile

Polymeric mesh endoprostheses “Lintex,” manufactured sterile under TU 9393-005-56257679-2006, are intended for various reconstructive surgical procedures. The product line includes the following versions:

Available Versions

• ESFIL® — polypropylene surgical mesh for reconstructive surgery; available in standard, lightweight, and heavyweight configurations. (Type 317100)
• UroSling® 1 — polypropylene mesh for reconstructive procedures. (Type 273970)
• UNIFLEX — polyvinylidene fluoride (PVDF) surgical mesh; available in standard, lightweight, and heavyweight configurations. (Type 317100)
• CARBOFLEX — PVDF surgical mesh with carbon coating; available in standard, lightweight, and heavyweight variants. (Type 317100)
• FLEXILEN — polypropylene–PVDF hybrid mesh for reconstructive surgery; available in standard, lightweight, and heavyweight options. (Type 317100)
• UroSling® — polypropylene–PVDF surgical mesh for reconstructive procedures. (Type 273970)
• ESLAN — polyester (lavsan) surgical mesh; available in standard and heavyweight configurations. (Type 317100)
• FTOREX® — polyester (lavsan) mesh with fluoropolymer coating for reconstructive surgery. (Type 317100)

All endoprostheses are supplied sterile and meet the requirements set forth by TU 9393-005-56257679-2006.

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The products posted on our website are approved for use in Russia by the state regulator Roszdravnadzor (Federal Service for Surveillance in Healthcare). The information is for informational purposes only.