A stent is a tempoary tubular device that is implanted in an artery to hold it open until the artery heals after a blockage is opened with balloon catheter (Percutaneous Coronary Intervention).
No. The resorbable stent is not for sale in any country. It is presently an experimental device that is only used in a laboratory setting.
The HARTLON resorbable stent is different from a metallic stent because it is made of a material that dissolves after the artery is healed leaving the artery in it natural state. The HARTLON resorbable stent is different from other resorbable scaffolds because its is made of a strong high molecular weight poly lactic acid that enables thin struts that slowly dismantle during resorption and its multilayer construct is designed to control the release rate of a therapeutic drug that minimizes scar tissue formation without interfering with the healing process.
HARTLON is providing the material described above for informational purposes only and that the material is not provided to you for the purpose of giving you medical advise, or instruction on the appropriate use of products described by HARTLON. You should not rely on the material in the FAQ in deciding on a treatment plan or in evaluating any other medical advise regarding any disease or medical condition, and HARTLON strongly urges that you consult with a qualified physician in connection with any and all treatment options that may be available to you. The device described on this FAQ is subject to Federal and International laws governing the use and sales of such devices, and is not approved for sale or clinical use for any indications. Nothing in this FAQ is intended to constitute a claim or indication for clinical uses of the devices described.
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