BEUDAMED
    4 results · 22ms · 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 ×

    FOLYSIL SILICONE CATHETER

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code EZL·August 2, 2023

    ARCHITECT ESTRADIOL

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code JLW·April 30, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 26, 2007

    DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HTO·October 11, 2012