Biodegradable Intestinal Bypass Stents from China Suppliers - Avoid Secondary Surgery | Factory Direct
PRODUCT FEATURES
It takes a short time for the anastomosis, technical methods are easy to master, and iterate products in the future are suitable for laparoscopic implementation.
Avoiding the anal fistula indwelled and the secondary surgery.
The physiological and psychological trauma of the patients is significantly reduced.
PRODUCT DESCRIPTION
| Product Use: | Applicable for bowel bypass surgery. |
| Product Highlights: | It is the first medical device in the world to protect the anastomotic stoma of low rectal cancer from stoma and reposition surgery. It can disintegrate and excrete from the body within 30 days. |
| Device Classification: | [CN] Class II |
| Material: | PGA, Barium Sulfate |
| Specification Description: | Different specifications represent the maximum diameters of anastomotic stents of 22 mm, 24 mm……38 mm |
| Storage Conditions: | The product shall be stored in an environment that is cool, dry, well-ventilated, clean with a relative humidity of not more than 80% and free of corrosive gases to avoid prolonged exposure to elevated temperatures. Do not expose the device to an environment over 40℃. |
PRODUCT SPECIFICATION
| Instructions: | Create an ileal incision 10 cm-15 cm from the ileocecal junction, place a product with appropriate size, and finally perform suture. Then place a drainage tube in the incision 10 cm proximal to the anastomosis. See the IFU for details. |
| Product advantages: |
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| Product structure and composition: | One-piece anastomosis stent |
| Precautions: |
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| Shelf life: | 2 years |
Frequently Asked Questions
What is the primary application of this biodegradable intestinal bypass stent?
This product is applicable for bowel bypass surgery. It is specifically designed to protect the anastomotic stoma of low rectal cancer from stoma and reposition surgery.
How long does the stent remain in the body and how is it removed?
The treatment duration is short, lasting about 2 to 4 weeks. Within 30 days (4 weeks) after surgery, the product gradually disintegrates in the intestinal tract and is excreted naturally from the body, leaving no residual foreign matters and avoiding secondary surgery.
Can the disintegration process of the stent be monitored?
Yes. The stent contains barium sulfate, which is radiopaque and can be developed under X-ray. This allows medical professionals to dynamically track its disintegration process.
What are the storage requirements for this medical device?
It should be stored in a cool, dry, well-ventilated, clean environment with a relative humidity of no more than 80%. It must be kept free of corrosive gases and protected from prolonged exposure to temperatures exceeding 40℃.
Are there any contraindications for using this stent?
Yes. The product is contraindicated in patients who require two or more intestinal anastomoses. Additionally, it is for single use only and must not be used by unskilled or untrained personnel, or if the package is damaged.

