BEUDAMED
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    QTY INVOLVED:

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 31, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019

    INSTRUMENT CASE, UNIVERS VAULTLOCK GLEN

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·May 1, 2024

    PEGGED GLENOID TRIL & DRILL GUIDE CADDY

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·June 17, 2024

    KEELED GLENOID TRIAL & DRILL GUIDE CADDY

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·June 14, 2024

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    COOLSCULPTING SYSTEM

    FDA Adverse Event
    Malfunction ·ALLERGAN PLEASANTON·Product code OOK·November 7, 2021

    PHILIPS SONICARE

    FDA Adverse Event
    Malfunction ·PHILIPS ORAL HEALTHCARE·Product code JEQ·July 24, 2018

    ARRAY SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code MNI·January 19, 2009

    ULTRASONIC DISSECTOR QTY

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code LFL·January 23, 2015

    C-TEK MAXAN ANTERIOR PLATING SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code KWQ·April 19, 2011

    S4 IMPLANTS, S4 POLYAXIAL SCREW

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code KWP·December 2, 2008

    CD HORIZON

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·July 20, 2021

    GUIDEWIRE ¿3.2 F/PFNA BLADE

    FDA Adverse Event
    Malfunction ·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code FZX·January 22, 2018

    DRILL BIT F/LATERAL CORTEX OPENING F/DHS

    FDA Adverse Event
    Malfunction ·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code HTW·January 10, 2018

    EBI SYNERGY SPINE SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, L.P.·Product code MNH·January 3, 2007

    CABLE CERCLAGE CABLE WITH CRIMP 1.8 MM DIA. 635 MM LENGTH

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KTT·December 31, 2019

    XPDM QUICK-CON SI POLY SCWDRVR

    FDA Adverse Event
    Malfunction ·DEPUY SPINE INC·Product code HXX·May 20, 2021