BEUDAMED
    6 results · 15ms · 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 ×

    ARTHREX ANGEL SYSTEM WITH ASPIRATION KIT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code ORG·May 1, 2019

    S-ROM*HEAD FEMORAL COCR 32+0

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code JDI·October 31, 2012

    ACTIVE ARTICULATION HIP SYSTEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·October 7, 2017

    M2A-MAGNUM MODULAR HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·April 6, 2017

    M2A-MAGNUM PF CUP 50ODX44ID

    FDA Adverse Event
    Injury ·.·Product code LPH·April 6, 2017

    M2A-MAGNUM PF CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·October 7, 2017