BEUDAMED
    10,000 results · 28ms · Sources: EU EUDAMED, US FDA

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    HOZ

    Device
    EU MDR · Eu Md Class 1 ·Sri Trang Gloves (Thailand) Public Company Limited·On the market

    HOZ

    Device
    EU MDR · Eu Md Class 1 ·Sri Trang Gloves (Thailand) Public Company Limited·On the market

    HOZ

    Device
    EU MDR · Eu Md Class 1 ·Sri Trang Gloves (Thailand) Public Company Limited·On the market

    HOZ

    Device
    EU MDR · Eu Md Class 1 ·Sri Trang Gloves (Thailand) Public Company Limited·On the market

    9600EMI

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·June 26, 2007

    9600EMI

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·June 26, 2007

    Fúróv.p. reteszcs-hoz átm.4,2 csigafúróhoz Troc.Z szeg

    Device
    EU MDR · Eu Md Class 1 ·Medimetál Gyógyászati Termékeket Gyártó és Forgalmazó Kft.·On the market·6 countries

    ONYX

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 4, 2025

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 4, 2025

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 14, 2024

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 13, 2025

    ONYX

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 13, 2025

    1047439-2002-00006

    FDA Adverse Event
    Other ·Product code HOZ·March 11, 2002

    1047439-2002-00007

    FDA Adverse Event
    Other ·Product code HOZ·March 11, 2002

    1047439-2002-00017

    FDA Adverse Event
    Other ·Product code HOZ·March 11, 2002

    1047439-2002-00008

    FDA Adverse Event
    Other ·Product code HOZ·March 11, 2002

    1047439-2002-00010

    FDA Adverse Event
    Other ·Product code HOZ·March 11, 2002

    1047439-2002-00013

    FDA Adverse Event
    Other ·Product code HOZ·March 11, 2002

    1047439-2002-00004

    FDA Adverse Event
    Other ·Product code HOZ·March 11, 2002

    LASIK EYE SPEAR

    FDA Adverse Event
    Injury ·BECTON-DICKINSON·Product code HOZ·March 11, 2002