BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    ORTHOPHOS 3/3 CEPH/3 DS

    FDA 510(k)
    FDA Class 2 ·Dental

    NONE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code UNK·December 11, 2009

    MariGen Wound Extra

    FDA 510(k)
    FDA Unclassified ·Unknown

    DUET LONG-TERM HEMODIALYSIS CATHETER SYSTEM, DUET LONG-TERM HEMODIALYSIS CATHETER SYSTEM CATHETER REPAIR KIT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TENOR SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWQ·December 11, 2009

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·March 5, 2013

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CARDIA CRT-D

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code NIK·August 8, 2014