BEUDAMED
    9 results · 37ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    PROSTHESIS, ELBOW, HEMI-RADIAL, POLYMER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code KWI·January 25, 2017

    2.4MM TI VA LOCKING SCREW STARDRIVE 24MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code HRS·June 17, 2016

    VEMO 31000-USA-QUADROX-I

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 25, 2014

    ATTAIN ABILITY PLUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·October 31, 2012

    PUMP MMT-522NAP PRDGM INS V2.2 PL EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·August 18, 2010

    8MM TI STRAIGHT RADIAL STEM 28MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code KWI·January 24, 2017

    22MM COCR RADIAL HEAD STANDARD HEIGHT/12.5MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code KWI·January 24, 2017

    18MM COCR RADIAL HEAD STANDARD HEIGHT/11.5MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code KWI·September 7, 2017

    7MM TI STRAIGHT RADIAL STEM 26MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code KWI·September 7, 2017