BEUDAMED
    25 results · 32ms · Sources: EU EUDAMED, US FDA

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    INDEPENDENCE SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACRY SMART 1ST

    FDA UDI
    DENTAL MANUFACTURING SPA·08056865121017·

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481122972·LOCATOR F-Tx Abutment for 4.1mm PrimaConnex Int...

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481115769·Attachment System, 4.1mm/4.5mm Internal TiLobe ...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946030988·X SERIES ADVANCED, MONITOR/DEFIBRILLATOR, 12 LE...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946050269·X SERIES MONITOR/DEFIBRILLATOR W/PACING, 12 LEA...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946060770·X SERIES ADVANCED, MONITOR/DEFIBRILLATOR, 12 LE...

    TIBIAL INSERT IMPACTOR TIP

    FDA Adverse Event
    Malfunction ·CONFORMIS, INC.·Product code OOG·April 28, 2017

    NA

    FDA UDI
    STERILMED, INC.·10888551032186·DRILL BIT SIDE CUTTING (SHANNON BUR) MEDIUM/M F...

    NA

    FDA UDI
    STRYKER CORPORATION·04546540077653·2.3mm Side Cutting Drill Bit

    GSP NEONATALGALT KIT, MODEL 3303-001U

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SURGIVISION MR COMPATIBLE VENTRICULAR CANNULA

    FDA 510(k)
    FDA Class 1 ·Neurology

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·May 31, 2001

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 16, 2025

    UNKNOWN PRODUCT - SET SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012

    BARD POWER GLIDE MIDLINE CATHETER M120101

    FDA Adverse Event
    Injury ·BARD·Product code FOZ·June 6, 2014

    HANDLE CEV1039-5-B DIA 5MM ANG [MXI/XOM]

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code GEI·May 14, 2013

    BIPOLAR HANDLE DIA 5MM ERG [MXI/XOM]

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S·Product code GEI·August 20, 2013

    ORTHO PROVUE

    FDA Adverse Event
    Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·February 6, 2017

    ANGIOVAC SUCTION CANNULA

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS·Product code DWE·May 13, 2013