The Bone Marrow Concentration System for Bone Graft Enrichment is an orthopedic medical device designed to facilitate the incorporation of autologous bone marrow components into bone graft materials during surgical procedures.
The system uses a negative-pressure enrichment mechanism to process the patient's own bone marrow together with bone repair materials, with the aim of incorporating biologically active components, including marrow-derived cells and growth factors, into the graft material.
It is intended for evaluation in orthopedic bone grafting procedures, particularly those involving bone defect repair and spinal fusion.
| Parameter | Description |
|---|---|
| Product Name | Bone Marrow Concentration System for Bone Graft Enrichment |
| Product Category | Orthopedic Medical Devices |
| Technology | Negative-Pressure Bone Marrow Enrichment |
| Biological Source | Autologous Bone Marrow |
| Intended Function | Enrichment of Bone Graft Materials |
| Main Applications | Bone Grafting, Bone Defect Repair, Spinal Fusion |
| Processing Principle | Cyclic Marrow Flow Through Bone Repair Materials |
| Product Model | To Be Confirmed |
| Device Dimensions | To Be Confirmed |
| Packaging Specification | To Be Confirmed |
| Sterilization Status | To Be Confirmed |
| Regulatory Documentation | Available upon manufacturer verification |
The system is designed to use the patient's own bone marrow as a source of biologically active components for bone graft preparation.
A cyclic negative-pressure mechanism is used to facilitate interaction between aspirated bone marrow and the selected bone repair material.
The system is designed to support the preparation of bone graft materials by incorporating components from autologous bone marrow.
Compatibility with individual graft materials must be confirmed by the manufacturer.
The device is described as a system for preparing bone graft material during an orthopedic surgical procedure.
The original product information identifies bone defect repair, large-segment bone grafting and long-segment spinal fusion as potential applications.
The manufacturer’s existing product information identifies the following application areas:
Bone defect reconstruction
Non-structural bone grafting procedures
Spinal fusion procedures
Large-segment bone tissue repair
Bone graft material preparation
Orthopedic procedures requiring bone graft enrichment
The final clinical indication must be confirmed against the manufacturer's approved instructions for use and the applicable regulatory authorization.
The system is based on a cyclic enrichment process involving autologous bone marrow and bone repair materials.
The existing manufacturer description outlines four general stages:
1. Preparation
The selected bone repair material is placed into the designated device chamber according to the manufacturer's instructions.
2. Autologous Bone Marrow Collection
Bone marrow is collected by qualified clinical personnel using an appropriate approved technique.
3. Cyclic Enrichment
The device uses a negative-pressure mechanism to facilitate contact between the collected bone marrow and the bone graft material.
4. Graft Material Preparation
Following the enrichment process, the prepared graft material may be used according to the surgical plan and the manufacturer's approved instructions for use.
Detailed procedural instructions, aspiration volumes, anticoagulant preparation and operating cycles must be taken from the current official instructions for use.
Overseas distributors and healthcare buyers may request information on:
Available models and product configurations
Material composition
Device operating principle
Sterilization and packaging
Shelf life and storage requirements
Manufacturer qualifications
Applicable product registration and certification
Clinical and performance evidence
Instructions for use
MOQ, lead time and export packaging
Document availability and regulatory status must be verified with the original manufacturer.
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Product availability and suitability for import depend on the manufacturer's documentation and the regulations of the destination market.
For technical documentation, available models, sample inquiries, distributor cooperation and commercial quotations, please contact:
ZHANMED LIMITED
Email: zhanmc@zhanmed.com
WhatsApp: +86 15215105391
For professional medical and institutional procurement inquiries. Product use is subject to the manufacturer's official instructions and applicable regulatory requirements.
Contact: Daniel Zhan
Phone: 18101053191
Tel: 02367309662
Email: zhanmc@zhanmed.com
Add: No.301, Unit 2, No.3 Building, No.7 Yard, Madian Xicun Road, Haidian District, Beijing China
Whatsapp: +8615215105391