BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RING

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

    MODIFICATION TO PREMIER III PHASED ARRAY CTL SPINE COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    Esperance Distal Access Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·January 28, 2013

    DUROM US ACETABAR COMPONENT 58/52 R

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWA·November 26, 2010

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 14, 2014

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·August 23, 2019

    VYPRO MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·August 23, 2019