BEUDAMED
    22 results · 31ms · 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 ×

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·March 30, 2026

    DRIVER SHAFT, T-15, LONG

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, LONG

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    3.0MM HEX DRIVER

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    SMS STEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·March 30, 2026

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·March 11, 2013

    PRECISION XTRA

    FDA Adverse Event
    Injury ·Product code NBW·February 27, 2011

    SETROX S 53

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO·Product code DTB·February 15, 2008

    UNIVERSAL GLENOID - CENTRAL SCREW 20MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·November 23, 2020

    UNI GLENOID-PERIPHERAL LOCK SCRW

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·November 23, 2020

    UNI GLENOID-PERIPHERAL LOCK SCRW

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·November 23, 2020

    HUM INSERT L/42+3 TO FIT IN 42 CUP CONST

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·November 23, 2020

    UNIVERS REVERS SPACER 42+12MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·November 23, 2020

    UNIVERS REVS CUP,42/+2MM LFT OFFSET CTD

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·November 23, 2020

    FIBERWIRE (TM) SUTURE KIT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GAT·November 23, 2020

    UNIVERSAL GLENOID - BASEPLATE SMALL

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·November 23, 2020