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 medical grade, 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
Senior Vice President, Coloplast
President, Urology Care
The Coloplast sling portfolio of Altis® Single Incision, Aris® Transobturator and Supris® Retrobpubic slings allow physicians to choose the sling and approach based on the patient. These slings are each kitted with ergonomic disposable introducers based on the approach.
The Coloplast sling portfolio is indicated for the treatment of female stress urinary incontinence (SUI) resulting from urethral hypermobility and/or intrinsic sphincter deficiency (ISD).