BEUDAMED
    6 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 ×

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE CR SIZE 5/10 MM R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·February 7, 2022

    INSET 30

    FDA Adverse Event
    Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·October 30, 2025

    LOGIC TIBIA PS MOD INSRT SZ 3 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 15, 2024

    WECK HEMOLOK ML CLIPS 6/CART 84/BOX

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDO·February 25, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code LWS·March 10, 2011

    REVITAN DIST. CURVED 18/200

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·August 11, 2014