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

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    COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·November 21, 2008

    CYPHER STENT

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NIQ·September 9, 2003

    PCA

    FDA Adverse Event
    Malfunction ·ABBOTT LABS - HPD·Product code MEA·May 18, 1999

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·June 8, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·September 10, 2015

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 17, 2014

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 10, 2013

    SUPRASORB X+PHMB

    FDA Adverse Event
    Death ·LOHMANN & RAUSCHER GMBH & CO·Product code MGQ·July 1, 2020

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LEH·October 31, 2013

    RADIATION

    FDA Adverse Event
    Injury ·Product code MUJ·June 16, 2014

    REMEDE SYSTEM

    FDA Adverse Event
    Injury ·ZOLL RESPICARDIA, INC..·Product code PSR·October 30, 2025

    SMARTSITE INFUSION SET AND SECONDARY SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·April 1, 2011

    BARD AMBULATORY PCA PUMP

    FDA Adverse Event
    Malfunction ·BARD·Product code MEA·July 20, 1992

    BARD AMBULATORY PCA PUMP

    FDA Adverse Event
    Malfunction ·BARD BARD AMBULATORY PCA PUMP·Product code MEA·July 20, 1992

    SAPPHIRE M.T INFUSION PUMP- US

    FDA Adverse Event
    Injury ·Q CORE MEDICAL LTD.·Product code FRN·July 7, 2016

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 29, 2013

    AIR EXPRESS LAL

    FDA Adverse Event
    Injury ·GAYMAR/PLEXUS·Product code FNM·December 6, 2013

    UNK CARDIOSEAL

    FDA Adverse Event
    Injury ·NMT MEDICAL, INC.·Product code MLV·February 8, 2003

    RESTYLANE LYFT WITH LIDOCAINE

    FDA Adverse Event
    Injury ·GALDERMA Q-MED AB·Product code LMH·September 9, 2020

    RESTYLANE LYFT WITH LIDOCAINE

    FDA Adverse Event
    Injury ·GALDERMA Q-MED AB·Product code LMH·September 9, 2020