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

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    DRAGER PT4000 PHOTOTHERAPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RUMI II KOH-EFFICIENT

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HEW·October 20, 2022

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009

    RAMP URINE HCG ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    INTERPORE CYLINDRICAL HEX IMPLANT

    FDA 510(k)
    FDA Class 2 ·Dental

    KOH-EFFICIENT,RUMI

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HEW·November 4, 2022

    KOH-EFFICIENT,RUMI

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC.·Product code HEW·November 3, 2022

    DRUG-ELUTING PERMANENT DEFIBRILLATOR ELECTRODES

    FDA Adverse Event
    Injury ·MPRI·Product code NVY·February 11, 2013

    PLM A+ PLATINUM MODU

    FDA Adverse Event
    Injury ·HOSPIRA, INC.·Product code FRN·December 15, 2010

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·July 17, 2014