BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    CALVITRON HAIR TRANSPLANT SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DeGen Medical Latitude-C AM Cervical Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Lite Touch

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

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MJK·May 19, 2014

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 7, 2011

    PINNACLE SECTOR II CUP 56MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·November 8, 2011

    PINNACLE MTL INS NEUT36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·February 27, 2012

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·February 27, 2012