Medical Skin Graft Mesher and Micrograft Expansion Carriers

Medical Skin Graft Mesher – Product Details

Product Components

• Main Unit: Medical skin graft mesher

• Accessories: Knife-holder handwheel, base, flattening components, tray, disc knife holder, and other supplied accessories. Final configuration is subject to the actual product package.

• Skin Graft Carrier: 42 × 42 mm cork carrier, with crepe-side and foil-side structures shown in the product materials.

Product Features

• Uniform Micrograft Preparation: Designed to support the organized cutting of skin grafts into a micrograft array.

• Multiple Expansion Options: Product materials indicate expansion ratios of 1:3, 1:4, and 1:6.

• Practical Carrier Design: The carrier supports micrograft arrangement, transfer, and expansion during the graft preparation process.

• Clinical Application References: Promotional materials reference burn care, trauma treatment, plastic and reconstructive procedures, and oncology-related skin grafting. Actual indications and intended use must comply with the applicable medical device registration certificate and Instructions for Use (IFU).

Technical Specifications

Note: Registration details, patent numbers, technical specifications, and product configuration should be verified against the current official documentation.

Operating Procedure Overview

1. Donor Site Preparation: Select the appropriate donor site and harvest the skin graft in accordance with established clinical procedures.

2. Graft Positioning: Place the harvested graft onto the cork carrier with the epidermal surface facing upward.

3. Initial Cutting: Position and secure the carrier in the device, then perform the first cutting pass according to the IFU.

4. Second Cutting Pass: Rotate the carrier or tray approximately 90° and complete the second pass as specified in the operating instructions.

5. Micrograft Expansion: Transfer the prepared micrografts to the designated expansion carrier and expand them in the required directions to the selected ratio.

6. Clinical Application: Complete graft placement and subsequent patient care in accordance with the applicable clinical protocols and current IFU.

Handling and Safety Precautions

• Qualified Operators Only: The device is intended for handling by trained healthcare professionals.

• Follow Official Instructions: Device preparation, carrier selection, cleaning, sterilization, and aseptic handling must comply with the current IFU and applicable institutional procedures.

• Verify Product Documentation: Confirm the applicable registration status, approved indications, supplied accessories, and technical specifications before clinical use.

• Clinical Outcome Disclaimer: Treatment outcomes depend on patient condition, clinical assessment, procedural technique, and postoperative care. No specific cure rate or complication rate is guaranteed.

Product Configuration and Documentation

The supplied accessories and carrier configuration are subject to the actual product package. Buyers and healthcare institutions should confirm the required configuration, applicable regulatory documentation, and current Instructions for Use with the supplier before ordering or using the device.