Dear Medical Professionals and Colleagues,
We know there is a lot of discussion surrounding the use of gynecological mesh, and you may have questions about the female pelvic health market and mesh devices as a therapy option.
At Coloplast, we greatly value our patients and physicians. Know that patient safety is our top priority. This also means we are deeply committed to maintaining quality throughout our supply chain.
Our gynecological mesh products are manufactured in the E.U. and U.S. in strict accordance with FDA and International quality and testing standards. They are made of biocompatible, knitted, non-absorbable, monofilament polypropylene mesh. We have great confidence in our products – the way they are designed and developed, the way they are manufactured, and the way they perform when used by a qualified surgeon with the appropriate patient.
Our mission at Coloplast is to make life easier for people with intimate healthcare needs. We firmly believe that women and their physicians should have a choice of therapies to successfully treat pelvic organ prolapse (POP) and stress urinary incontinence (SUI), and believe the medical devices in today’s marketplace deliver on that.
Know that Coloplast remains committed to you and Female Pelvic Health therapies.
President, Coloplast Interventional Urology
Coloplast’s prolapse solutions are designed to support transvaginal or transabdominal techniques and include Restorelle® Y-Mesh, Flat Mesh, and DirectFix. The portfolio also includes Axis™ and Suspend® allograft as well as various accessories to help with these surgical approaches.
To learn more about the symptoms, causes, and diagnosis of pelvic organ prolapse, visit FemalePelvicSolutions.com.