BEUDAMED
    146 results · 14ms · Sources: EU EUDAMED, US FDA

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    Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement. Do not reuse. Ethylene Oxide Sterilized. Made in the U.S.A. Synovis Surgical Innovations A division of Synovis Life Technologies, Inc., 2575 University Ave. W., St. Paul, MN 55114-1024 USA.

    FDA Recall
    Terminated ·Synovis Surgical Inovation Div. of·Product code FTM·November 1, 2005

    XenMatrix Surgical Graft Sterile, Porcine Dermal Matrix 19 x 28 cm Rectangle Catalog #: 1161928

    FDA Recall
    Terminated ·Davol, Inc., Sub. C. R. Bard, Inc.·Product code FTM·January 7, 2011

    Gynecare PROLIFT Total Pelvic Repair System PFRT01 Ethicon Deutschland

    FDA Recall
    Terminated ·Ethicon, Inc. US·Product code FTM·April 20, 2007

    Synovis Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement, (PSD 28-U-V), 28mm, US Surgical Staplers. Each package contains the following components: Cartridge and anvil assemblies, Cartridge cone, PSD Gel, & C-clip

    FDA Recall
    Terminated ·Synovis Surgical Inovation Div. of·Product code FTM·March 16, 2007

    OviTex 1S Reinforced BioScaffold 6x10cm, Part Number F10256-0610G

    FDA Recall
    Terminated ·AROA Biosurgery, LTD.·Product code FTM·April 6, 2018

    OviTex Reinforced BioScaffold 10x12cm, Part Number F10254-1012G

    FDA Recall
    Terminated ·AROA Biosurgery, LTD.·Product code FTM·April 6, 2018

    Strattice Reconstructive Tissue Matrix for Stoma Reinforcement. 8 cm x 8 cm Packaged in an inner foil pouch inside outer foil pouch tertiary carton. LifeCell Corporation, One Millennium Way, Branchburg, NJ 08876 Strattice is intended for use as a foil tissue patch to reinforce soft tissue where weakness exists and for the surgical repair of damaged or ruptured soft tissue membranes. It is used for repair of hernias and/or body wall defects which require the use of reinforcing or bridging material to obtain the desired surgical outcome. It is intended for single patient one time use.

    FDA Recall
    Terminated ·LifeCell Corporation·Product code FTM·July 12, 2010

    AMS InteXen LP Collagen Dermal Matrix, REF 72404066. Product Size: 8 x 12 cm. AMS InteXen LP is a sterile non-perforated processed porcine collagen dermal matrix. Sterile EO. American Medical Systems, Inc., 10700 Bren Road West, Minnetonka, MN 55343 USA. The AMS collagen dermal matric is intended for use in the treatment of hernias where connective tissue has ruptured or for implantation to reinforce soft tissues where weakness exists in the urological, gynecological, or gastroenterological anatomy.

    FDA Recall
    Terminated ·American Medical Systems·Product code FTM·December 5, 2008

    MatriStem Plastic Surgery Matrix XS Intended for implantation to reinforce tissue where weakness exists in urological, gynecological, and gastrointestinal anatomy, including, but not limited to the following procedures: pubourethral support, tissue repair, body wall repair, and esophageal repair

    FDA Recall
    Terminated ·ACell, Inc·Product code FTM·July 7, 2011

    OviTex Reinforced BioScaffold 6x10cm, Part Number F10254-0610G

    FDA Recall
    Terminated ·AROA Biosurgery, LTD.·Product code FTM·April 6, 2018

    OviTex Reinforced BioScaffold 16x20cm, Part Number F10254-1620G

    FDA Recall
    Terminated ·AROA Biosurgery, LTD.·Product code FTM·April 6, 2018

    OviTex Reinforced BioScaffold 18x22cm, Part Number F10254-1822G

    FDA Recall
    Terminated ·AROA Biosurgery, LTD.·Product code FTM·April 6, 2018

    OviTex Reinforced BioScaffold 10x20cm, Part Number F10254-1020G

    FDA Recall
    Terminated ·AROA Biosurgery, LTD.·Product code FTM·April 6, 2018

    Peri-Strips Dry with Veritas Collagen Matrix Staple Line Reinforcement (PSDV), sterile EO, Rx Only, Synovis Surgical Innovations, A Division of Synovis Life Technologies, Inc, 2575 University Ave W., St Paul, MN 55114-1024. The device is intended to be used as a staple line buttress

    FDA Recall
    Terminated ·Synovis Surgical Inovation Div. of·Product code FTM·October 26, 2011

    OviTex 1S Reinforced BioScaffold 20x20cm, Part Number F10256-2020G

    FDA Recall
    Terminated ·AROA Biosurgery, LTD.·Product code FTM·April 6, 2018

    OviTex 2S Reinforced BioScaffold 10x12cm, Part Number F10258-1012G

    FDA Recall
    Terminated ·AROA Biosurgery, LTD.·Product code FTM·April 6, 2018

    OviTex 1S Reinforced BioScaffold 16x20cm, Part Number F10256-1620G

    FDA Recall
    Terminated ·AROA Biosurgery, LTD.·Product code FTM·April 6, 2018

    OviTex 2S Reinforced BioScaffold 6x10cm, Part Number F10258-0610G

    FDA Recall
    Terminated ·AROA Biosurgery, LTD.·Product code FTM·April 6, 2018

    Synovis Peri-Strips Dry with Veritas Collagen Matrix Circular Staple Line Reinforcement,( PSD 21-E-V), 21mm, Ethicon Circular stapler. Each package contains the following components: Cartridge and anvil assemblies, Cartridge cone, PSD Gel, & C-clip.

    FDA Recall
    Terminated ·Synovis Surgical Inovation Div. of·Product code FTM·March 16, 2007

    Peri-Strips Dry with Veritas Collagen Matrix Staple Line Reinforcement (PSD-V), 4506 ETS-V. PSD-V is an implantable surgical mesh comprised of non-crosslinked bovine pericardium in a dehydrated form. Do not reuse. Consult Instructions for Use. Sterilized. Product treated with sodium hydroxide. Produt derived from USDA-inspected cattle. Made in the U.S.A. Rx Only. Synovis Surgical Innovations A Division of Synovis Life Technologies, Inc., 6575 University Ave W., St. Paul, MN 55114-1024 USA. 651 796-7300, 800.487.9627

    FDA Recall
    Terminated ·Synovis Surgical Inovation Div. of·Product code FTM·May 23, 2005