BEUDAMED
    33 results · 25ms · Sources: EU EUDAMED, US FDA

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    ALPHA MICRON 20 MICROAGGREGATE FILTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Zuma

    FDA UDI
    Seaspine Orthopedics Corporation·10889981097158·Drill Handle, AO Connect

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867062504·UNIVERS REVERS SPACER 36+15MM

    ZOETIC GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MULTICHECK(TM)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    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

    TherMax Blood Warmer Unit-US, PrisMax Accessory, Product Codes: 955630, 955515, 955702, 955631

    FDA Recall
    Open, Classified ·VANTIVE US HEALTHCARE LLC·Product code KDI·July 28, 2025

    TherMax Blood Warmer Unit-US, PrisMax Accessory, Product Codes: 955630, 955515, 955702, 955631

    FDA Enforcement
    Class II ·Ongoing·VANTIVE US HEALTHCARE LLC·September 3, 2025

    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