Biodegradable Intestinal Anastomosis Stent Stapler - No Residue, China Suppliers & Factory Available

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Place of Origin Made in China
Brand Name Biodegradable intestinal anastomosis stent
Certification ISO13485
Model Number BIS22-H, BIS24-H, BIS26-H, BIS30-H, BIS34-H, BIS38-H

Product Detail

PRODUCT FEATURES

Within 4 weeks after surgery, the product can gradually disintegrate in the intestinal tract and excrete from the body, without residual foreign matters.

It contains barium sulfate, which can be developed under X-ray, so its disintegration process could be dynamically tracked.

The suture should be reduced or even avoided, and the integrity of intestinal wall and blood supply would be ensured to the greatest extent, which is conducive to the healing of anastomotic stoma and preventing the occurrence of anastomotic leakage.

PRODUCT DESCRIPTION

Product Use	Applicable for intestinal anastomosis.	Product Highlights	It is the first Intestinal anastomosis device in the world to effectively protect the blood supply of anastomotic stoma, facilitate physiological healing, and avoid the occurrence of anastomotic leakage. 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	Disconnect the intestinal canal, use a professional intestinal diameter gauge to measure the inner diameter of intestinal canal, select a product of appropriate size to place in the intestinal lumen at the broken end, and finally perform suture. See the IFU for details.
Product advantages	• Short anastomosis time, no damage to anastomotic submucosal vessels; • Within 4 weeks after surgery, the product can gradually disintegrate in the intestinal tract and excrete from the body, without residual foreign matters in the body; • The product contains barium sulfate, which can be developed under X-ray, so its disintegration process is allowed to be dynamically tracked; • It is easy to operate, conforms to physiology, disintegrates on time, and effectively avoids complications.
Product structure and composition	One-piece anastomosis stent
Precautions	• The product is for single use; it is not designed to be used in case of damaged package. • The product must not be used by unskilled or untrained personnel. • It is contraindicated in patients requiring two or more intestinal anastomoses.
Shelf life	2 years

Frequently Asked Questions (FAQ)

What is the primary application of this intestinal anastomosis device?

The device is specifically applicable for intestinal anastomosis. It helps connect segments of the intestinal canal while protecting the blood supply of the anastomotic stoma to facilitate physiological healing.

How long does it take for the device to disintegrate and leave the body?

The device is designed to gradually disintegrate in the intestinal tract and be excreted from the body within 4 weeks (30 days) after surgery, leaving no residual foreign matters.

Can the post-surgery disintegration process of the stent be monitored?

Yes. Because the device contains barium sulfate, it can be visualized under X-ray, allowing medical professionals to dynamically track its disintegration process.

What materials are used to manufacture this anastomosis stent?

The product is composed of PGA (Polyglycolic Acid) and Barium Sulfate, structured as a one-piece anastomosis stent.

What are the specific storage requirements for this product?

It must be stored in a cool, dry, well-ventilated, and clean environment with a relative humidity of not more than 80% and free of corrosive gases. Avoid exposure to environments exceeding 40℃.

Are there any contraindications for using this device?

Yes, the device is contraindicated in patients who require two or more intestinal anastomoses. Additionally, it is for single use only and must not be used by untrained personnel.