Bone growth repair fusion marrow concentrator

  • Bone Marrow Concentration System for Bone Graft Enrichment
Bone Marrow Concentration System for Bone Graft Enrichment

Bone Marrow Concentration System for Bone Graft Enrichment

  • Product Type: Bone Marrow Enrichment System
  • Application: Bone Grafting
  • Procedure: Spinal Fusion / Bone Defect Repair
  • Technology: Negative-Pressure Enrichment
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Bone Marrow Concentration System for Bone Graft Enrichment

Product Overview

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.

Product Information

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

Product Features

1. Autologous Bone Marrow-Based Enrichment

The system is designed to use the patient's own bone marrow as a source of biologically active components for bone graft preparation.

2. Negative-Pressure Enrichment Technology

A cyclic negative-pressure mechanism is used to facilitate interaction between aspirated bone marrow and the selected bone repair material.

3. Integration with Bone Graft Materials

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.

4. Intraoperative Preparation Concept

The device is described as a system for preparing bone graft material during an orthopedic surgical procedure.

5. Orthopedic Application Focus

The original product information identifies bone defect repair, large-segment bone grafting and long-segment spinal fusion as potential applications.

Intended 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.

Working Principle

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.

Technical and Regulatory Documentation

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.

International Supply and Sourcing Support

Zhanmed Limited supports international buyers seeking orthopedic medical devices and related medical products from qualified Chinese manufacturers.

Our services include:

  • Supplier sourcing and coordination

  • Technical specification communication

  • Sample and product documentation requests

  • Commercial quotation coordination

  • Export documentation and logistics follow-up

  • International distributor cooperation

Product availability and suitability for import depend on the manufacturer's documentation and the regulations of the destination market.

Request a Quotation

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.