BEUDAMED
    198 results · 24ms · Sources: EU EUDAMED, US FDA

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    MONTAGE Settable, Resorbable Hemostatic Bone Putty

    FDA 510(k)
    FDA Unclassified ·Unknown

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756628044·Air/Gel Stirrup

    ANKLE BRACE STIRRUP SMALL

    FDA UDI
    Bird & Cronin, LLC·00610570176014·

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707013853·CALIBRA 1ST MOL BANDS W/G8325-02 n.UR 5

    BLUEENDO

    FDA UDI
    TROKAMED GmbH·04251303822097·Trocar, conical blunt Ø 15 mm for protective sl...

    Geneva

    FDA UDI
    Nucletron B.V.·08717213055995·Intrauterine Tube 0mm

    Engage Partial Knee System

    FDA UDI
    Engage UNI LLC·B6951520050000·Right Tray

    ALLURA XPER OR TABLE SERIES

    FDA 510(k)
    FDA Class 2 ·Radiology

    R&R EXTERNAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Herbert/Whipple®

    FDA UDI
    Zimmer, Inc.·00889024033771·

    MINIMALLY INVASIVE SOLUTIONS TECHNOLOGY OFFSET RASP HANDLE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LXH·October 28, 2005

    SOF-FLEX DOUBLE PIGTAIL STENT SET

    FDA Adverse Event
    Injury ·COOK UROLOGICAL, INC.·Product code FAD·October 19, 2005

    MICROLAB AT PLUS 2

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code JTC·March 14, 2006

    VENTAK PRIZM AVT

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code DXY·May 9, 2006

    TRILOGY ACETABULAR SYSTEM LINER

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LPH·October 13, 2005

    DUAL LUMEN INSERTION TRAY

    FDA Adverse Event
    TYCO/KENDALL HEALTHCARE·Product code LJS·November 15, 2005

    MICROSPAN SYSTEM

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code FED·July 15, 2005

    CERAMTEC CERAMIC INS/SLEEVE TRIDENT H

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MRA·October 17, 2005

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·September 29, 2005

    INRATIO

    FDA Adverse Event
    Injury ·HEMOSENSE, INC.·Product code GIS·February 6, 2006