BEUDAMED
    215 results · 41ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    LINOX SD 60/16

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code LWS·September 15, 2009

    THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·September 17, 2022

    ELOX EX 60-BP

    FDA Adverse Event
    Injury ·BIOTRONIK, GMBH AND CO.·Product code DTB·July 14, 2009

    ELOX EX 45-BP

    FDA Adverse Event
    Injury ·BIOTRONIK, GMBH AND CO.·Product code DTB·July 14, 2009

    PHILOS DR

    FDA Adverse Event
    Injury ·BIOTRONIK, GMBH AND CO.·Product code DXY·July 14, 2009

    COROX OTW 85-BP

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code NKE·January 20, 2012

    LUMAX 740 HF-T

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code NIK·April 10, 2014

    BIOTRONIK

    FDA Adverse Event
    Injury ·BIOTRONIK INC.·Product code DXY·March 10, 2004

    BIOTRONIK BIOMONITOR 3M LOOP RECORDER

    FDA Adverse Event
    Injury ·BIOTRONIK INC.·Product code MXD·April 9, 2021

    BIOTRONIK PACEMAKER/DEFIBRILLATOR

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code MRM·June 24, 2022

    DEXTRUS 4135

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code NVZ·June 22, 2012

    LINOX SMART S DX 65/15

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code LWS·May 4, 2012

    SETROX S 60

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code DTB·May 4, 2012

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code DTB·June 22, 2012

    DEXTRUS 4135

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code NVZ·June 22, 2012

    DEXTRUS 4135

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code NVZ·February 6, 2012

    EDORA 8 DR-T

    FDA Adverse Event
    Injury ·BIOTRONIK INC.·Product code NVZ·November 1, 2017

    BIOTRONIK EVIA DR-T

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code NVZ·June 7, 2021

    DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code NVN·July 25, 2024

    PERMANENT DEFIBRILLATOR ELECTRODES

    FDA Adverse Event
    Injury ·BIOTRONIK, INC.·Product code DTB·August 27, 2024