BEUDAMED
    14 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VENTRALIGHT ST W/ ECHO

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·July 17, 2024

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 30, 2026

    BI-METRIC/X POR NC 11X135

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 13, 2018

    M2A 38MMX50MM CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    BP ADVANCED PERSONAL DOUBLE

    FDA Adverse Event
    Malfunction ·MEDELA, INC.·Product code HGX·June 25, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 11, 2013

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 29, 2026

    M2A 38MM MOD HD+9MM NK NO SKRT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 26, 2025

    VENTRALIGHT ST W/ ECHO

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·October 14, 2020

    TERUMO RADIFOCUS GUIDE WIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 3, 2025

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 21, 2018

    VENTRALIGHT ST W/ ECHO

    FDA Adverse Event
    Death ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·February 20, 2018