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

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    RETINA ANGIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LITTER, NONRIDGID, POLELESS, NYLON STRETCHER

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MODEL 490-01 PACING LEAD

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    PRIMUS HI

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC., RADIATION ONCOLOGY·Product code IYE·January 10, 2013

    STERLING BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·January 3, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 18, 2014

    JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023

    JAWS "HIQ+", 5 X 330 MM, SCISSORS, METZENBAUM

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 30, 2023

    SHAFT "HIQ+", 5 X 330 MM

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·May 23, 2023

    JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023