BEUDAMED
    24 results · 67ms · Sources: EU EUDAMED, US FDA

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    MEDVANCE SILICONE FOAM, BOARDERED SILICONE FOAM DRESSING

    FDA Adverse Event
    Injury ·MED WAY INC.·Product code NAD·June 5, 2023

    FORCE FX GENERATOR

    FDA Adverse Event
    VALLEYLAB, INC.·Product code GEI·May 10, 2000

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LNM·January 30, 2012

    NOVA MIGHTY MACK ROLLATOR

    FDA Adverse Event
    Malfunction ·NOVA ORTHO-MED INC.·Product code ITJ·April 26, 2013

    DELTAFILL18 3MM X 12CM

    FDA Adverse Event
    Malfunction ·REFER TO SECTION H10·Product code KRD·July 25, 2018

    PERFUSOR SPACE

    FDA Adverse Event
    Malfunction ·B.BRAUN MELSUNGEN AG·Product code FRN·November 13, 2022

    BAND AID BRAND KPP (KIZU POWER PAD) BANDAGES

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code NAD·September 9, 2022

    BAND AID BRAND KPP (KIZU POWER PAD) BANDAGES

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code NAD·September 9, 2022

    BAND AID BRAND KPP (KIZU POWER PAD) BANDAGES

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON CONSUMER INC·Product code NAD·September 9, 2022

    TEMPO

    FDA Adverse Event
    Malfunction ·ARJO MED AB LTD·Product code FSA·November 6, 2014

    DELTAXSFT10 2.5MM X 6CM

    FDA Adverse Event
    Malfunction ·REFER TO SECTION H10·Product code KRD·November 1, 2018

    MK1 POOL LIFT

    FDA Adverse Event
    Other ·ARJO MED AB LTD.·Product code FSA·September 23, 2012

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 29, 2016

    MK1 POOL LIFT

    FDA Adverse Event
    Malfunction ·ARJO MED. AB LTD·Product code FSA·September 15, 2017

    MARISA

    FDA Adverse Event
    Malfunction ·ARJO MED. AB LTD.·Product code FSA·April 20, 2016

    NEO-FIT NEONATAL ENDOTRAC

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code JAY·February 5, 2019

    PROGAV 2.0 SYS PED.WITH PRECHAMBER

    FDA Adverse Event
    Malfunction ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·August 31, 2018

    PROSA VALVE

    FDA Adverse Event
    Malfunction ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·August 31, 2018

    ESSURE

    FDA Adverse Event
    Injury ·BAYER·Product code HHS·May 6, 2014

    BONE SCREW 76353200 REPOSE SYSTEM

    FDA Adverse Event
    Death ·INFLUENT MEDICAL, LLC·Product code LRK·April 18, 2012