BEUDAMED
    25 results · 29ms · 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 ×

    CD 3700 SL

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 23, 2007

    TRANSVENE

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code LWS·February 11, 2013

    TENDRIL ST

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

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 24, 2014

    UNI GLENOID-PERIPHERAL LOCK SCRW

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·October 28, 2020

    UNIVERSAL GLENOID - CENTRAL SCREW 15MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·October 28, 2020

    UNIVERS REVERS SPACER 36+15MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·October 28, 2020

    UNIVERS REVERS GLENO 36 +4 LAT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·October 28, 2020

    UNI GLENOID-PERIPHERAL LOCK SCRW

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·October 28, 2020

    UNIVERS REVERS STEM, SIZE 7, CAP COATED

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·October 28, 2020

    FW,BPB #2 SUTR,BLU W/NDL

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GAT·October 28, 2020

    #5 FIBERWIRE W/ NEEDLES FOR SUTUREPLATE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code GAT·October 28, 2020

    UNIVERS REVS CUP,36/NEUTRAL CTD

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·October 28, 2020

    UNIVERSAL GLENOID - BASEPLATE SMALL

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·October 28, 2020

    HUMERAL INSERT S/36 +3 TO FIT IN 36 CUP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·October 28, 2020

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·September 19, 2024

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·September 19, 2024

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·September 19, 2024

    UNIVERS REVERS HUMERAL STEM, SIZE 9

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSD·June 25, 2024

    UNIVERS REVERS FRACTURE ADAPTER TRUNION

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSD·June 25, 2024