BEUDAMED
    611 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·March 24, 2012

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·February 1, 2012

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·February 10, 2012

    OSS AVL TIBIAL LOCK RING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·April 14, 2026

    PT2 MODERATE SUPPORT GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC SCIMED, INC.·Product code LOX·June 19, 2006

    SPECTRANETICS ELCA LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORPORATION·Product code LPC·August 8, 2013

    NEUWAVE PR XT PROBE 20CM 15GA

    FDA Adverse Event
    Injury ·NEUWAVE MEDICAL, INC.·Product code NEY·December 20, 2021

    SEG HINGE POST, SZ F 14MM 3DEG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·February 21, 2022

    STEM COLLAR 35 MM O.D.

    FDA Adverse Event
    Injury ·ZIMMER TMT·Product code JWH·August 16, 2018

    DEPUY SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC.·Product code KWS·December 6, 2017

    SEG TM COLLAR

    FDA Adverse Event
    Injury ·ZIMMER TRABECULAR METAL TECHNOLOGY·Product code JWH·October 26, 2011

    SEG-WAY ECUTR

    FDA Adverse Event
    Injury ·TRICE MEDICAL, INC.·Product code LXH·October 18, 2022

    SEG-WAY ECUTR

    FDA Adverse Event
    Injury ·TRICE MEDICAL, INC.·Product code LXH·January 30, 2026

    OSS AXLE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·January 19, 2018

    OSS REINFORCED YOKE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·January 19, 2018

    JETSTREAM XC ATHERECTOMY CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MCW·March 7, 2019

    1030489-2015-03390

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·December 14, 2015

    1030489-2015-03386

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·December 14, 2015

    SEGMENTAL FLUTED STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·July 10, 2024

    SEGMENTAL FLUTED STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPAEDIC MFG. LTD.·Product code LZO·April 2, 2024