BEUDAMED
    5 results · 28ms · 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 ×

    INTER-LOCK SCREWDRIVER T25/3.5MM HEX/224MM

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·October 13, 2020

    3.5MM TI CANCELLOUS POLYAXIAL

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MNI·December 7, 2010

    ZEPHYR XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 8, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·December 7, 2012

    EU 4.5X22MM STENT 12 MM DW TIP

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code NJE·August 25, 2022