BEUDAMED
    5 results · 16ms · 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 ×

    REGEN/RNGLC+ MULTI 56MM SZ 24

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWZ·March 20, 2018

    ARCOS CON SZ E HI 80MM HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 20, 2018

    ARCOS 20X190MM SPL TPR DIST HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 20, 2018

    36MM COCR BIOMET FEM HD +6 NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·September 7, 2018

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·September 16, 2011