BEUDAMED
    8 results · 27ms · 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 ×

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code EZW·October 8, 2012

    LOCK SELF-CENTERING HEAD Ø47

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LPH·September 19, 2022

    CEMENTED GLENOID 3 PEGS SMALL

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A·Product code KWS·June 16, 2023

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·August 26, 2013

    EVOLVE

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH, INC.·Product code IKY·May 2, 2014

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 7, 2013

    UNKNOWN MESH PRODUCT (EWHU)

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·November 10, 2010

    1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015