MEUS-1511 cerabone® 500-1000micron, 1.0ml / 1.0cc
Product Code: MEUS-1511
- MEUS-1510 cerabone® 500-1000micron, 0.5ml / 0.5cc
- MEUS-1512 cerabone® 500-1000micron, 2.0ml / 2.0cc
- MEUS-1515 cerabone® 500-1000micron, 5.0ml / 5.0cc
- MEUS-1520 cerabone® 1000-2000micron, 0.5ml / 0.5cc
- MEUS-1521 cerabone® 1000-2000micron, 1.0ml / 1.0cc
- MEUS-1522 cerabone® 1000-2000micron, 2.0ml / 2.0ml
- MEUS-1525 cerabone® 1000-2000micron, 5.0ml / 5.0cc
- Particle Size (µm) : 500-1000
- Volume (ml) : 1
- Origin : Bovine
ULTIMATE VOLUME STABILITY, SUPERIOR HYDROPHILICITY, CE MARKING SINCE 2002
cerabone® is a 100% pure bone mineral of bovine origin manufactured by a unique 1200°C production process. It has been successfully applied in millions of patients in regenerative dentistry and has been in use for more than 20 years in various medical applications (e.g. craniofacial surgery, oncology, and hand and spine surgery).
MAXIMUM SAFETY
The sophisticated processing of the bovine bone removes all organic components resulting in a bone mineral with exceptional purity. In addition, potential infectious agents such as bacteria, viruses, and prions are removed through high-temperature treatment. Both product and production processes are fulfilling applicable national and international regulatory and safety requirements for bovine bone grafts including ISO 22422-1, ISO 22442-2, & ISO 22442-3.
Generally, the high stability of cerabone® makes it the ideal choice in cases where long-term stability is important. IMPLANTOLOGY, PERIODONTOLOGY, AND ORAL AND CMF SURGERY
ADVANTAGES
- 100% pure natural bone mineral
- Human-like bone structure
- Rough, hydrophilic surface
- Ultimate volume stability
- Easy handling
INDICATIONS
- Sinus lift
- Horizontal and vertical augmentation
- Ridge preservation
- Peri-implant defects
- Socket preservation
- Bone defect augmentation
- Periodontal intrabony defects
- Furcation defects (class I and II)
To our valued customers in Canada: Please note this item is currently not available in Canada as it is awaiting approval by Health Canada.
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Choice of Particle Size:
Small cerabone® particles (0.5 – 1.0 mm) allow good adaptation to surface contours; they are especially useful for lateral augmentations or to fill voids when working with autologous bone blocks. For sinus lift and extensive augmentations, the use of large cerabone® particles (1.0 – 2.0 mm) is recommended. The increased space between the large particles enables better vascularization and improves the regeneration of larger defects.
Hydration:Cerabone® granules can be applied dry or wet. Hydration in blood or sterile saline solution facilitates the handling and application of the granules, as they adhere to each other.
Compacting of the granules:
To provide space for the regenerative process only gentle compression of the granules is recommended. It allows for revascularization and osseointegration of the bone grafting particles by the three-dimensional pore network of cerabone®.
Stabilization of the granules:
The cerabone® granules should always be covered by a membrane to immobilize the particles at the augmented site and prevent soft tissue ingrowth into the bone defect. When treating defects outside the ridge contour, a fixation of the membrane by pins or screws can be advantageous.
Healing time and re-entry:
A healing time of at least 6 months is recommended before re-entry to ensure stable integration of the particles.
Mixing with autograft:
Mixing of cerabone® with autologous bone adds a biological activity (osteoinductive and osteogenesis properties of autologous bone) and supports faster regeneration and improved formation of new bone.
Mixing with allograft (maxgraft®):
Mixing of cerabone® with allogeneic bone (maxgraft®) combines the advantages of both materials; the biological potential of maxgraft® and the long-term stability of cerabone® lead to fast regeneration of vital, strong bone.