SMARTBRANE SIMPLE RELIABLE PURE NEW! Resorbable Pericardium Membrane MORE ECONOMIC. THE SMALLEST MEMBRANE 10 x 10 mm. 10 x10

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SMARTBRANE Resorbable Pericardium Membrane 10 x10 NEW! THE SMALLEST MEMBRANE 10 x 10 mm SIMPLE RELIABLE PURE MORE ECONOMIC

SIMPLE Optimized handling properties ensuring straight-forward application The supercritical carbon dioxide (scco 2 ) cleaning process is gently removing unwanted materials (e.g. cells, lipids) while preserving the natural collagen matrix as well as the natural crosslinking of the collagen fibers. 1,2 As a result, SMARTBRANE is characterized by optimal material stability as the biomechanical characteristics of porcine pericardium tissue are preserved. 3 NEW MINI! 10 x 10 mm 15 x 20 mm 20 x 30 mm 30 x 40 mm SMARTBRANE... features an adequate tensile strength is very adaptable to bony surfaces without sticking to the graft or instrument is very thin (< 0,4mm) for facilitated augmentation and wound closure ECONOMIC MORE ECONOMIC The smallest membrane 10 x 10 mm SMARTBRANE is a resorbable collagen membrane made of porcine pericardium. Thus, it features all benefits of a modern native collagen membrane. In addition to the standard membrane sizes, it is available in a mini format of 10 x 10 mm. This offers a more economic membrane solution especially for regeneration of small bone defects to optimize your cost-benefit structure. 10 x10 NEW! THE SMALLEST MEMBRANE 10 x 10 mm SMARTBRANE rehydrated: Excellent adaptation to surfaces without sticking to graft or instrument. 3

PURE Excellent biocompatibility for improved wound healing SMARTBRANE is manufactured using an innovative and highly effective cleaning technology based on supercritical carbondioxide (scco 2 ). This process results in a higher purity and creates a biocompatible base for immediate new bone ingrowth. 1,2 It provides highest possible biocompatibility characteristics due to it s porcine origin and the scco 2 cleaning process. SMARTBRANE cross-section (magnification x 40) featuring intact structure as well as a natural interconnective porous system. Histological examination in vivo 4 RELIABLE Natural collagen matrix preserved by scco 2 cleaning technology for enhanced graft performance SMARTBRANE is made of porcine pericardium and thus presents optimal matrix composition and a natural dense 3D-network collagen structure optimally preserved after scco 2 purification. The preserved natural collagen matrix plays an important role for blood clotting and promotes cell attachment. 5 The membrane has a resorption time of 8-12 weeks providing adequate barrier function for usage in standard GBR cases. 6 After 1 week of subcutaneous implantation in a rat muscle: SMARTBRANE (M) is already connected to the muscular tissue (MT), no signs of inflammatory reactions. After 2 weeks the first blood vessels (BV) are invading SMARTBRANE (M), no signs of inflammatory reactions. 5

REPORT CASE REPORT Augmentation of a dehiscence-type defect around dental implant TECHNOLOGY scco 2 cleaning process as basis for optimal matrix properties and maximal graft safety STEP 1 scco 2 Processing STEP 2 Chemical Treatment STEP 3 Freeze-Drying STEP 4 -Sterilization Surgery Dehiscence defect around bone level implant. STEP 1 Supercritical Carbon Dioxide (scco 2 ) Processing Carbon dioxide is in its supercritical state when both the temperature and pressure equal or exceed the critical point of 31 C and 73 atm. In this supercritical state, CO 2 has both gas-like and liquid-like qualities. By it s effective tissue perfusion and removing capabilities of unwanted substances it provides ideal conditions for cleaning and sterilising tissues. 1,2 Furthermore, scco 2 is known to be highly efficient against all kinds of pathogens. 7 Augmentation with Xenograft bone. Step 2 Chemical Treatment Various chemical treatment steps are applied to provide a pure membrane matrix by inactivating and removing residual non-collagenous proteins and enzymes. This results in a further increased safety level for pathogen inactivation. 8 Coverage of bone graft material with SMARTBRANE the membrane can be easily positioned and is adapting ideally to the defect geometry. Step 3 Freeze-Drying Freeze-drying allows gentle preservation, retaining the original 3D structure of the xenograft. After freeze-drying, products can be stored at room temperature and generally have a longer shelf-life. Suture removal Optimal initial healing pattern: no signs of irritation. Step 4 Gamma-Sterilization The combination of scco 2 cleaning process and terminal gamma-sterilization provides highest possible viral and bacterial inactivation and results in a sterile (SAL>10-6 ) and highly biocompatible bone graft. 1,9 7

REFERENCES 1. Nichols A, Burns DC, Christopher R. Studies on the Sterilization of Human Bone and Tendon Muscoskeletal Allograft Tissue Using Supercritical Carbon Dioxide. Journal of Orthopaedics 2009. 2. Sawada K, Terada D, Yamaoka T, Kitamura S, Fujisato T. Cell removal with supercritical carbon dioxide for acellular artificial tissue. J Chemical Technol Biotechnol 2008;83(6):943 949. 3. Internal testing results, data on file. 4. SMARTBRANE subcutaneous implantation test, data on file. 5. Brett D. A Review of Collagen and Collagen-based Wound Dressings. Wounds 2008;20(12). 6. Internal testing results, data on file. 7. a. Pages F, Poirier B, Barbier Y, Frayssinet P, Joffret M-L, Majewski W, Bonel G, Larzul D. Viral Inactivation of Human Bone Tissue using supercritical Fluid Extraction. ASAIO Journal 1998;44:289-293. 7b. Qiu QQ, Leamy P, Brittingham J, Pomerleau J, Kabaria N, Connor J. Inactivation of bacterial spores and viruses in biological material using supercritical carbon dioxide with sterilant. J Biomed Mater Res B Appl Biomater. 2009;91(2):572-8. 7c. Dillow AK, Dehghani F, Hrkach JS, Foster NR, Langer R. Bacterial inactivation by using near- and supercritical carbon dioxide. Proc Natl Acad Sci U S A. 1999;96(18):10344-8. 8. Sofer G, Lister DC, Boose JA. Part 6, Inactivation Methods Grouped by Virus. BioPharmInternational 2003;6 Supplement:S37-S42. 9. Thomas FC, Ouwerkerk T, McKercher P. Inactivation by gamma irradiation of animal viruses in simulated laboratory effluent. Appl Environ Microbiol. 1982;43(5):1051 1056. Clinical pictures by courtesy Dr. Kai Fischer (Germany). Manufactured by REGEDENT AG, Zollikerstrasse 144, CH - 8008 Zürich CE0086 Version 150818 CONTACT