BEUDAMED
    30 results · 22ms · Sources: EU EUDAMED, US FDA

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    ROCHE ONLINE GENTAMICIN

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·34546540602542·Bone Screws, MP, Cross-Pin

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065692·INTRAORAL ELASTICS 4,5 oz 3/16" green

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481122859·LOCATOR R-Tx Attachment System, 5.0mm Platform ...

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221231352·Unitek Miniature Twin MBT UR Lateral 8T/8A 022 MMT

    DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    KSEA MINIATURE NEUROENDOSCOPE

    FDA 510(k)
    FDA Class 2 ·Neurology

    WARMTOUCH COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCOHEALTHCARE·Product code DWJ·August 30, 2011

    WARMTOUCH COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code DWJ·January 12, 2011

    WARMTOUCH COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code DWJ·April 28, 2011

    PROMUS PREMIER

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·October 15, 2020

    WARMTOUCH COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code DWJ·August 30, 2011

    WARMTOUCH COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO·Product code DWJ·July 29, 2011

    WARMTOUCH COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code DWJ·May 25, 2011

    WARM TOUCH COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN/ FORMERLY TYCO HEALTHCARE·Product code DWJ·January 6, 2011

    WARMTOUCH COMPACT WARMING UNIT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code DWJ·September 2, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·December 30, 2015

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·May 1, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWP·August 1, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·May 15, 2013