Intepro mesh
WebOct 29, 2014 · Primary Aim: The primary aim of this randomized controlled trial (RCT) is to compare vaginal mesh and suture exposure rates in women undergoing robotic total … WebThe first two studies utilized IntePro (mesh density 50 g/m (2)) and the third utilized IntePro Lite (mesh density 25.2 g/m (2)). Data were pooled to form IntePro and IntePro Lite …
Intepro mesh
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WebFor EACH AMS Women’s Pelvic Mesh Device implanted you MUST provide: A copy of the product identification sticker(s) (PID) OR if a copy or copies of the PID is/are not available … http://www.amsmeshclassactions.ca/faq.aspx
WebMar 15, 2012 · IntePro Lite was employed in all cases. It is a type I macroporous polypropylene mesh with the same knit as IntePro (as seen in Apogee), possessing a … WebJul 27, 2012 · Need Legal Help Regarding IntePro Transvaginal Mesh? The personal injury attorneys at Parker Waichman LLP offer free, no-obligation case evaluations. For more …
WebOct 2, 2011 · Each mesh system is intended to remain in the body as a permanent implant and is not absorbed or degraded by the action of ingrowth or tissue enzymes. Preoperatively, patients received intravenous cephalosporin or quinolone within an hour of surgery. Operative techniques for Perigee and Apogee were as previously described [ 24, 30 ]. Webpolypropylene mesh; (iv) the implants contained in the Elevate Apical and Posterior Prolapse Repair System (the Elevate Apical and Posterior Implant) which were made of IntePro™ Lite, non-absorbable polypropylene mesh; (Group Members who had surgery to implant one or more of the Mesh Implants being the Mesh Sub-Group Members); and/or
Brand Name: IntePro Y-Mesh Version or Model: 72404000 Commercial Distribution Status: Not in Commercial Distribution Catalog Number: 72404000 Company Name: ENDO PHARMACEUTICALS INC. Primary DI Number: 00814723020333 Issuing Agency: GS1 Commercial Distribution End Date: March 31, 2016 Device Count: 1
WebSep 26, 2016 · ("surgical mesh"/OR (mesh* OR 4DDOME OR AIGISRx OR AlloDerm OR AlloMax OR "Bard Composix EX" OR "BIO-A Tissue Reinforcement prosthesis" OR CollaMend OR DermaMatrix OR DualMesh OR "Evolution P3EM" OR FasLata OR FlexHD OR FortaGen OR "IntePro Lite" OR InteXen OR NEOVEIL OR "Parietex composite" OR Pelvicol OR Pelvisoft … dr andreas temmelWebPerigee system with IntePro mesh used in the study. All of the surgeons already had expe-rience with using this macroporous type I soft polypropylene mesh. Dr. Moore presented 12-month data on 96 of the 114 patients studied. Twenty-three percent (22) had prior cystocele repair, 87% (83) were postmenopausal, and 54% (52) had a prior hysterectomy ... dr andrea stern mount joy family medicineWebApr 1, 2024 · Mesh erosion is a serious and not uncommon complication in women undergoing vaginal mesh repair. We hypothesized that mesh erosion is associated with … dr andrea stephens obWebIllinois Department of Transportation Bureau of Materials QUALIFIED PRODUCT LIST SYNTHETIC FIBERS January 21, 2024 This list supersedes the May 21, 2024 list. dr andreas thalheimerWebAug 29, 2012 · Device Name: IntePro® Y-Mesh Indications for Use: The IntePro® Y-Mesh is intended for use in vaginal prolapse repair via abdominal sacrocolpopexy procedures, … dr. andrea stephensWebAug 10, 2012 · A California woman has filed a defective vaginal mesh lawsuit against American Medical Systems (AMS) alleging she was seriously injured by the company’s Monarc Subfascial Hammock and Apogee System with Intepro mesh devices. dr andrea stewartWebOct 17, 2006 · The Prolapse Registry was an observational study of patients who were implanted with AMS devices for the surgical repair of female pelvic prolapse. The registry followed patients post-operatively for up to 2 years and collected demographic, clinical, surgical, safety, and patient outcomes data. dr. andreas teufer