BEUDAMED
    32 results · 23ms · Sources: EU EUDAMED, US FDA

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    COPAN VIRAL TRANSYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092131190·Biomet 3i Certain®-compatible 4.1mm 17° Multi-U...

    HI-TORQUE BALANCE MIDDLEWEIGHT

    FDA UDI
    ABBOTT VASCULAR INC.·08717648013836·HI-TORQUE BALANCE MIDDLEWEIGHT Guide Wire .014 ...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092104323·Biomet 3i Certain®-compatible 4.1mm 17° Multi-U...

    HI-TORQUE BALANCE MIDDLEWEIGHT

    FDA UDI
    ABBOTT VASCULAR INC.·08717648025969·HI-TORQUE BALANCE MIDDLEWEIGHT Guide Wire w/Hyd...

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008774·PedFuse Respond, CNL, 9.0mm x 80mm

    SPINE SYSTEM EVOLUTION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TEMPORARY PACEMAKER EXTENSION CABLE, MODELS 5235, 5235A, 5235V, TEMPORARY PACEMAKER SURGICAL EXTENSION CABLE, MODELS 528

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HI-TORQUE GUIDEWIRE 1001780-HC

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code DQX·July 23, 2025

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 26, 2012

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 26, 2012

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·October 15, 2009

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·December 31, 2009

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·October 29, 2009

    PUMP IN STYLE ADVANCED BREAST PUMP BACKPACK

    FDA Adverse Event
    Malfunction ·MEDELA, INC.·Product code HGX·February 11, 2013

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 3, 2011

    INDURA

    FDA Adverse Event
    Malfunction ·MEDTRONIC VASCULAR·Product code LKK·February 19, 2008

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 21, 2010

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 21, 2010

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·August 13, 2010