BEUDAMED
    5 results · 23ms · 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 Status: Injury ×

    LUMAX 340 VR-T

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code LWS·November 12, 2010

    3.0MM TI-SCREWANCHOR1BLUE SUTU

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·May 4, 2018

    3.0MM TI-SCREWANCHOR1BLUE SUTU

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·March 15, 2018

    3.0MM TI-SCREWANCHOR1BLUE SUTU

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·March 12, 2018

    3.0MM TI-SCREWANCHOR1BLUE SUTU

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·May 4, 2018