BEUDAMED
    5 results · 24ms · 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 ×

    BONE SPREADER 12MM BEAK WIDTH

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWN·April 18, 2024

    AMISTEM-P STD STEM SIZE 5

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·April 15, 2020

    CALCIUM GEN. 2

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CHW·June 30, 2014

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·November 10, 2010

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·January 4, 2013