BEUDAMED
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    PORE-SI BONE GRAFT SUBSTITUTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TruLock

    FDA UDI
    Rmo, Inc.·00885797644930·TRULOCK Primer Activated Adhesive Kit (40 Capsule)

    Disposable Cuff

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935103431·

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NQW·August 10, 2017

    ERECAID CLASSIC SYSTEM; ERECAID ESTEEM MANUAL SYSTEM; ERECAID ESTEEM BATTERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    D.O.R.C. HARMONY TOTAL TTC VITRECTOMY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    CENTERPIECE? PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code NQW·April 16, 2015

    CENTERPIECE¿ PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·June 8, 2016

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·December 7, 2017

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·July 28, 2019

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·July 28, 2019

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NQW·May 22, 2019

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NQW·May 22, 2019

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·June 11, 2020

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NQW·March 1, 2018

    CENTERPIECE PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code NQW·February 22, 2018

    CHATANOOGA VECTRA NEDEK 2761

    FDA Adverse Event
    Injury ·DJO GLOBAL·Product code IPF·April 2, 2013

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·April 5, 2011

    PERCUFLEX PLUS URETERAL STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·May 7, 2008

    CENTERPIECE CONNECT PLATE FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NQW·July 6, 2021