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

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    Filters FDA Adverse Event ×

    IMMULITE 2000 3GALLERGY SPECIFIC IGE

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code DHB·May 22, 2018

    IMMULITE 2000 3GALLERGY SPECIFIC IGE

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code DHB·May 22, 2018

    INTIMA-II Y 24GAX0.75IN PRN/EC SLM

    FDA Adverse Event
    Injury ·BD (SUZHOU)·Product code FOZ·May 11, 2021

    QC Ø1-4 F/TRS

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWE·March 26, 2013

    SYNCHRON® LX RHEUMATOID FACTOR (RF REAGENT)

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code DHR·March 17, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·March 25, 2008

    ANATOMICAL SHOULDER REVERSE, HUMERAL INSERT, PE, 36-3

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSD·November 10, 2021

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·Product code FOZ·July 19, 2021