BEUDAMED
    49 results · 38ms · Sources: EU EUDAMED, US FDA

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    FDA Adverse Event
    Malfunction ·CORTEX INC.·Product code DQK·January 14, 2026

    FLEXIMARC G/T¿

    FDA Adverse Event
    Malfunction ·CORTEX MANUFACTURING INC.·Product code NEU·July 9, 2019

    TECNIS SIMPLICITY

    FDA Adverse Event
    Malfunction ·AMO MANUFACTURING NETHERLANDS·Product code MFK·August 1, 2025

    CONVENTUS PHS SYSTEM

    FDA Adverse Event
    Malfunction ·CONVENTUS ORTHOPAEDICS, INC.·Product code JDS·September 4, 2020

    CONVENTUS PHS SYSTEM

    FDA Adverse Event
    Malfunction ·CONVENTUS ORTHOPAEDICS, INC.·Product code JDS·September 4, 2020

    CONVENTUS PHS SYSTEM

    FDA Adverse Event
    Malfunction ·CONVENTUS ORTHOPAEDICS, INC.·Product code JDS·September 4, 2020

    FIBERLOCK SUSPENSION SYSTEM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·June 7, 2024

    TECNIS SIMPLICITY

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code HQL·April 22, 2022

    FIBERTAK

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·June 3, 2024

    TIGHTROPE ® II RT WITH DEPLOYING SUTURE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·April 24, 2024

    FIBERTAK BICEPS IMPLANT SET

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·June 20, 2024

    BTB TIGHTROPE W/ DEPLOYING SUTURE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTY·April 9, 2024

    DEPTH GAUGE FOR 3.5MM CORTEX SCREWS

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTJ·November 16, 2021

    IMPLANT SYSTEM, FIBERTAK BUTTON

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·May 21, 2024

    TECNIS SIMPLICITY

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code HQL·February 4, 2021

    UNK CR FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HSA·August 31, 2010

    UNKNOWN NEXGEN COMPLETE KNEE SOLUTION LEGACY POSTERIOR STABILIZED (LPS) FEMORAL

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HSA·December 11, 2008

    DBL LD DX FBR TK W/BLK, 0.9MM ST NDLS

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·May 16, 2024

    NATURAL KNEE PATELLA DRILL GUIDE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HTW·March 1, 2011

    ACL TIGHTROPE WITH FIBERTAG

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MBI·May 31, 2024