The membrane is made from natural, highly purified type I and III collagen and bovine elastin. Possesses the increased durability and moderate extensibility.
It is indispensable for carrying out operations of scientific and technological revolution and NCR.
It has two dissimilar surfaces - smooth and fleecy.
The high strength and elasticity of the membrane allows it to be fixed at the implantation site without damaging the structure. Creates a barrier after planting the osteoplastic material and prevents soft tissue migration. The controlled and standardized manufacturing technology of the product guarantees biocompatibility, lack of immune response and stable clinical performance with predictable results.
Membrella® Barrier Membrane bioresorbable, which avoids surgery to remove it, and consequently, additional trauma to the patient.

Membrella® -Barrier
xeno - P E R I C A R D I U M

Membrane biocompatibility has been repeatedly proven in experimental studies, and the effectiveness is confirmed by the results of clinical use. Publications describing the results of using this product can be found in the "Publications" section. With the Membrella® - PERICARDIUM Barrier membrane, your bone grafting will always be protected.

• GBR-guided bone regeneration (horizontal augmentation)
• GBR-guided bone regeneration (vertical augmentation)
• Mechanical barrier against soft tissue migration
• Alveolar process reconstruction
• Stabilization of blood clot
• Fixation of osteoplastic material
• Closure of sinus perforations
• Closure of mandibular canal perforations

• No fixation often required due to hydrophilicity
• High tensile strength
• Stable graft support
• Protects graft from soft tissue ingrowth
• Heals by secondary intention if exposed

Origin: xeno
Thickness: 0.3 – 0.5 mm
Elasticity: stretch
Resorption: 14 – 24 weeks
Layers: 2
Strength: 910 mg
Surface heterogeneity: Yes

• 20 × 15 mm
• 20 × 30 mm
• 25 × 25 mm
• 30 × 40 mm
• 25 × 40 mm