Compared with traditional open surgery, percutaneous minimally invasive surgery is less invasive and less invasive

The channel tool is used to create minimally invasive channels.
It has lateral and head / tail extension functions.
The channel is visible and equipped with light source system.
Y-type optical cable can be connected to arthroscope / cold light source machine / special charging power supply system.
It can be used for single-stage and multi-stage channel establishment.
It can be used for intervertebral treatment and pedicle screw

Diameter(mm):5.0,5.5,6.0,6.5,7.0
Length(mm):35,40,45,50,55

1. Please carefully read the instruction before use.
2. Before the surgery, determine the surgery plan according to the symptom, sign and the image check.
3. MR examination can be carried out onTi6Al4V product according to routine parameters of the hospital.
4. Choose the products and special matching tools with suitable specification and model according to the symptom and the position of patients.
5. Perform the surgery under the directions of an experienced surgeon.
6. The surgeon shall describe the relevant precautions in details to the patients before the surgery.
7. At the delivery time, if the product is found scratched, damaged, and bended or cracked, it cannot be used anymore.
8. The implants and tools provided by our company are not sterilized but the devices must be sterilized before the surgery. We recommend the method of high pressure steaming for sterilization.
9. Any activities in the early post-operation period, if being conducted improperly in method or extent, would possibly cause the invalidation of the metal implant, such as fixation loosening, broken or bending, etc. For this reason, the time, method and extent of activity in the early post-operation period shall be conducted strictly under the correct instruction of the surgeon, and shall be implemented step by step.
10. Before healing of bone grafting in early post-operation period, the external fixation shall be used for 6 to 12 weeks.
11. The product is disposable.
12. And it is forbidden to be used with products of other materials and model or from other companies.
13. To avoid contamination, this product should be disposed as infectious medical waste disposal method.

1.The products and instruments should be sterilized before use. Recommended to meet the EN ISO 17665-1 related requirements of the high pressure steam sterilization method. Recommended sterilization conditions:Down-draining steam sterilizer: temperature: 121℃; duration of exposure: 30 minutes; barometric pressure: 102.9kPa(1.05kg/cm2); drying time:45 minutes. High pressure steam sterilizer must be approved by the hospital and inspection regularly to ensure the medical device can reach the recommended sterilization temperature during the exposure period.
2.The product is disposable and should not be reused under any circumstances. Used implants may contain many acquired flaws, or the integrity of itself may be damaged, which will shorten the service life or cause cross infection. Whether