BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    LORENZ EXTERNAL MANDIBULAR DISTRACTOR

    FDA 510(k)
    FDA Class 2 ·Dental

    SX-One MicroKnife

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    REVERSE SHOULDER PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATIA)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KNW·June 7, 2006

    LINOX SMART SD 60/16

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code LWS·March 1, 2013

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 5, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014