BEUDAMED
    595 results · 46ms · Sources: EU EUDAMED, US FDA

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    BIOTRONIK, INC.

    FDA registration
    BIOTRONIK, INC.·25 products·🇺🇸 United States

    BIOTRONIK NRO, INC.

    FDA registration
    BIOTRONIK NRO, INC.·1 product·🇺🇸 United States

    BELOS VR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH & CO.·Product code MKJ·July 24, 2003

    BELOS VR

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH & CO.·Product code MKJ·July 24, 2003

    BELOS VR-T

    FDA Adverse Event
    Other ·BIOTRONIK GMBH & CO.·Product code LWS·September 30, 2003

    BELOS VR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH & CO.·Product code LWS·September 30, 2003

    BELOS DR-T

    FDA Adverse Event
    Other ·BIOTRONIK GMBH & CO.·Product code LWS·September 30, 2003

    BELOS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH & CO.·Product code LWS·September 30, 2003

    DEIKOS A+

    FDA Adverse Event
    Other ·BIOTRONIK GMBH & CO.·Product code LWS·April 30, 2004

    TACHOS DR

    FDA Adverse Event
    Other ·BIOTRONIK GMBH & CO.·Product code MRM·April 30, 2004

    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

    SETROX S 45

    FDA Adverse Event
    Other ·BIOTRONIK GMBH AND CO.·Product code DTB·September 12, 2008

    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

    GUARDIAN SYSTEM

    FDA Adverse Event
    Malfunction ·AVERTIX MEDICAL INC.·Product code QBI·June 2, 2025

    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