BEUDAMED
    18 results · 38ms · Sources: EU EUDAMED, US FDA

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    Arthrex DynaNite Nitinol Staple

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    External Fixation

    FDA UDI
    Life Spine, Inc.·00190837023232·Rancho Cube, 5 Hole

    CAREFUSION NICOLET EDX

    FDA 510(k)
    FDA Class 2 ·Neurology

    OSTEOGRAF/D-300

    FDA 510(k)
    FDA Class 2 ·Dental

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

    STELLARIS ELITE VISION ENHANCEMENT SYSTEM

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQC·March 1, 2022

    25 GA POSTERIOR WIDE-FIELD ELITE PACK

    FDA Adverse Event
    Malfunction ·BAUSCH + LOMB, INC·Product code HQC·December 6, 2019

    ARTICULEZE M 28MM 1.5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code JDI·September 17, 2013

    PINNACLE MTL INS NEUT28IDX50OD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWA·September 17, 2013

    PHILIPS BURTON MEDICAL PRODUCTS

    FDA Adverse Event
    Malfunction ·PHILIPS BURTON MEDICAL·Product code FTD·July 18, 2011

    EXOSEAL VASCULAR CLOSURE DEVICE (VCD)

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code MGB·June 17, 2013

    PULMONETIC

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 203/PULMONETIC SYSTEMS, INC.·Product code CBK·September 17, 2008

    STELLARIS POWER SUPPLY II

    FDA Adverse Event
    Malfunction ·BAUSCH + LOMB·Product code HQC·August 1, 2023

    SROM 28MM +0 M HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC USA·Product code JDI·July 24, 2012

    PINNACLE MTL INS NEUT28IDX50OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC USA·Product code KWA·July 24, 2012

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 15, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·June 28, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·March 5, 2021