BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    ProLite Mesh, ProLite Ultra Mesh, ProLoop Mesh Plug

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

    ProLift Trial

    FDA UDI
    Life Spine, Inc.·00190837087753·

    CML 1000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SPEEDFIX SUTURE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERSAFITCUP DM HC LINER Ø 48

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·September 30, 2015

    ACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Injury ·ROCHE DIABETES CARE AG·Product code LZG·June 7, 2013

    CENTURY

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 8, 2011

    WHEELCHAIR, BARIATRIC, 26", REM F

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES, INC.·Product code IOR·September 5, 2008

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 11, 2019

    Medical Linear Accelerator

    FDA Enforcement
    Class II ·Terminated·Elekta, Inc.·September 14, 2016