BEUDAMED
    27 results · 24ms · Sources: EU EUDAMED, US FDA

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    CONCORDE CURVE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SELF CENTERING

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295003564·SELF CENTERING BI-POLAR HEAD 22.225mm ID 43mm OD

    ATLAS SPINE PIVOTING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHES MODIFIED BIORESORBABLE SUTURE ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·October 24, 2015

    VA LOCKSCR Ø2.4 SELF-TAP L12 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 18, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 9, 2013

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH LTD./HUNTINGTON·Product code HQL·May 19, 2011

    MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·August 8, 2008

    VA LOCKSCR Ø2.7 HEAD 2.4 SELF-TAP L14 TA

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·April 27, 2022

    FIAB EURODEFIPADS

    FDA Adverse Event
    Malfunction ·FIAB S.P.A.·Product code LDD·October 19, 2022

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 30, 2015

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HWC·December 30, 2014

    UNK - SCREWS: 2.7 MM VA LOCKING

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·March 1, 2024

    EURODEFIPADS

    FDA Adverse Event
    Malfunction ·FIAB SPA·Product code LDD·April 19, 2023

    DIRECTINJECT ON DEMAND HA CEMENT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-LIMERICK·Product code GXP·March 10, 2016

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 22, 2016

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 12, 2016

    DEFICOM

    FDA Adverse Event
    Malfunction ·FIAB SPA·Product code LDD·December 21, 2023

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·October 24, 2015