BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    MINIARC PRO SINGLE-INCISION SLING SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LARGE CANNULATED SCREWS

    FDA UDI
    Smith & Nephew, Inc.·03596010063960·6.5MM UNIVERSAL CANNULATED SCREW 105MM

    Phantom® Fibula Nail System

    FDA UDI
    Paragon 28, Inc.·00889795146496·1.6mm x 400mm, Entry Guidewire, Ball Tip

    XTD THROMBECTOMY CATHETER, XX CM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AG THERMOGRAPHIC CAMERA, MODEL ATIR-M301

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    HYDRATOME

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code KNS·March 29, 2007

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR CLONMEL·Product code NIQ·June 18, 2010

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code MGB·June 27, 2022

    STARTER GUIDEWIRE

    FDA Adverse Event
    Malfunction ·LAKE REGION MEDICAL LIMITED·Product code DQX·May 5, 2026

    HEARTMATE II SYSTEM CONTROLLER

    FDA Adverse Event
    Malfunction ·THORATEC CORP.·Product code DSQ·May 9, 2013

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Injury ·BAXTER HEATHCARE CORPORATION·Product code FKX·September 26, 2014

    SIG MOD TIB TRAY CEM COCR 3

    FDA Adverse Event
    Injury ·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code JWH·June 2, 2011