BEUDAMED
    2,649 results · 34ms · Sources: EU EUDAMED, US FDA

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    ASTRA-OCT Spine System

    FDA UDI
    SPINECRAFT, LLC·00193082161643·ASTRA-OCT Dedicated Reduction Polyaxial Screwdr...

    ASTRA Spine System

    FDA UDI
    SPINECRAFT, LLC·00193082155758·ASTRA Dedicated Reduction Polyaxial Screwdriver...

    IMPlate

    FDA UDI
    SKELETAL DYNAMICS L.L.C.·00841506102122·

    IMPlate

    FDA UDI
    SKELETAL DYNAMICS L.L.C.·00841506102115·

    MediMax Tech

    FDA UDI
    MEDIMAX TECH INC.·00817325020800·DRN Rocker Button ESU Pencil - 2.5'' Stainless ...

    UNKNOWN INSERT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·July 18, 2017

    I-STAT DOWNLOADER, NETWORK

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code RHA·October 7, 2017

    I-STAT DOWNLOADER, NETWORK

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code RHA·June 16, 2017

    I-STAT DOWNLOADER RECHARGER, NETWORK

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JQP·February 13, 2024

    TECNIS SIMPLICITY

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code MFK·April 3, 2026

    COULTER® ACT 8/10 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·November 12, 2012

    I-STAT DOWNLOADER, NETWORK

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code RHA·September 19, 2017

    COULTER® ACT DIFF 12¿ ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·December 28, 2012

    LOCKABLE DRAINAGE LINE

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·October 23, 2023

    WRIST ARTHRODESIS NAIL SYSTEM

    FDA Adverse Event
    Other ·SKELETAL DYNAMICS LLC·Product code HSB·November 14, 2011

    TRIDENT 0° X3 INSERT 36MM ID

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·May 10, 2013

    JP PERF DRN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code GBX·July 3, 2024

    LRG TAP ORI MOD NCK 0DEG 38MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS - CORK·Product code MEH·September 5, 2012

    LINKSYMPHOKNEE

    FDA Adverse Event
    Malfunction ·WALDEMAR LINK GMBH & CO. KG·Product code HRY·June 1, 2023

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL MANUFACTURING CORPORATION·Product code MVK·June 23, 2015