SYNERGY - Bovine Pericardum Membrane 20x30mm Resorbable 4-6 months - # SY-MP 23-05
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Description
Bovine Pericardum SYMP-23-05
DESCRIPTION
SYNERGY Bovine pericardium Membrane, reference SYMP-23-05, Bovine Pericardum SYMP-23-05. A Resorbable collagen-based barrier Membrane derived from Bovine pericardial tissue, used in guided bone regeneration (GBR) and guided tissue regeneration (GTR) procedures.
The pericardium's dense collagen-fiber architecture provides extended barrier function compared to thinner collagen membranes, supporting bone-graft containment during the regenerative phase.
CLINICAL APPLICATION
Used as a barrier Membrane over bone-graft material in regenerative procedures associated with implant dentistry — extraction-socket preservation, ridge augmentation, sinus elevation, peri-implant defect repair, and periodontal regeneration. The extended resorption profile of pericardium-derived membranes is well suited to larger defects requiring longer barrier function during the bone-formation phase.
PLATFORM & COMPATIBILITY
Pairs with particulate bone grafts (xenograft / allograft / autograft) in conventional GBR workflows. Consult the SYNERGY clinical literature for case-specific protocols and practitioner judgement for defect-specific use.
TECHNICAL SPECIFICATIONS
| Manufacturer reference | SYMP-23-05 |
|---|---|
| Brand | SYNERGY |
| Product family | Bovine Pericardium Membrane |
| Designation | Bovine Pericardum SYMP-23-05 |
| Format | Pre-cut sheet — per size designation in name (mm) |
| Material | Bovine pericardium — processed collagen-fiber matrix |
| Resorption profile | Extended (typically 4–6 months) |
| Indication | GBR / GTR — barrier Membrane for bone and soft-tissue regeneration |
| Regulatory | CE marking · ISO 13485 medical-device QMS |
MATERIALS & SURFACE
Manufactured under controlled biological processing conditions designed to preserve the natural collagen structure and mineral matrix of the source tissue. Lot-controlled production with full traceability from raw material origin through final packaging.
Supplied terminally sterilized using validated methods appropriate to the biological substrate.
STERILIZATION & HANDLING
Supplied sterile, single-use, in primary and secondary protective packaging. Do not re-sterilize. Use only if the sterile barrier is intact at the time of opening. Storage at room temperature, away from direct sunlight and moisture; observe the printed expiration date.
Discard unused product after the procedure per local biohazard regulations. Verify lot number and expiration date prior to clinical use.
QUALITY ASSURANCE
Manufactured under ISO 13485 medical-device quality management and supplied with CE marking for the European market. Each lot is documented with origin traceability, processing parameters and sterility validation records.