BEUDAMED
    22 results · 21ms · Sources: EU EUDAMED, US FDA

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    MEDPOR CUSTOMIZED SURGICAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Harvard PremiumFill OptiTips A1

    FDA UDI
    Harvard Dental International GmbH·EHAR70836211·Universal light cure nano-hybrid composite for ...

    ZAVATION

    FDA UDI
    Zavation LLC·00842166157149·HA+ ALIF 8deg 36mmx21

    ZAVATION

    FDA UDI
    Zavation LLC·00842166154926·WHITNEY 8deg 36mmx21mm

    Zavation

    FDA UDI
    Zavation LLC·00842166106154·ALIF 8deg 36mmx21

    Zavation

    FDA UDI
    Zavation LLC·00842166180598·ALIF Sizer 8deg 36mm x 21mm

    ST/AR ST AND ARRHYTHMIA SOFTWARE, MODEL RELEASE D.0

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD SAF-T PRN LUER ACTIVATED VALVE, MODEL 385100

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SINAI HSP BALTIMORE MD 1

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DTZ·July 6, 2011

    LAKELAND REG LAKELAND FL 1

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DWF·May 3, 2010

    WA ADVENT TAKOMA PARK MD 1

    FDA Adverse Event
    Other ·SORIN GROUP USA, INC.·Product code DTZ·November 22, 2011

    IOWA METH DES MOINES IA1

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA, INC.·Product code DTZ·March 7, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·April 29, 2013

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 29, 2008

    CONCERTO CRT-D DR AT

    FDA Adverse Event
    Death ·MEDTRONIC S.A.·Product code NIK·May 10, 2011

    BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 31, 2019

    Q-SYTE CLOSED LUER ACCESS DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·November 13, 2020

    BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 8, 2022

    11MM/130 DEG TI CANN TFNA 380MM/RIGHT - STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HSB·March 28, 2017

    BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·March 7, 2018