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

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    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·July 23, 2021

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·May 14, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 28, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 28, 2021

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·May 14, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 8, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·February 19, 2021

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·BIOFORM MEDICAL, INC.·Product code LMH·July 15, 2009

    LINER AND SHELL WITH PLASTIC BARRIER 48 MM I.D. 60 MM O.D.

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 3, 2023

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 20, 2013

    STEALTHSTATION TREON TREATMENT GUIDANCE SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·February 3, 2011

    ENTRUST AT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·March 10, 2008

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 28, 2021

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·April 8, 2021

    S.M.A.R.T. NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·July 31, 2015

    S.M.A.R.T. NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·July 31, 2015

    S.M.A.R.T. NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·July 31, 2015