BEUDAMED
    10,000 results · 73ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    QardioBase 2

    FDA UDI
    QARDIO, INC.·00854894005241·

    INTERVENTIONAL FLUOROSCOPIC X-RAY SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC (LITTLETON)·Product code OWB·December 18, 2018

    REFURBISHED PULSAR I GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·January 26, 2016

    GE OEC 9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 30, 2008

    ASCENT - BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code MJN·December 18, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 3, 2007

    RELAY THORACIC STENT-GRAFT WITH PLUS DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOLTON MEDICAL, INC.·Product code MIH·January 4, 2021

    CARDIOSAVE HYBRID, TYPE G PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·February 29, 2024

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·December 24, 2008

    LITHODIAMOND LITHOTRIPTER

    FDA Adverse Event
    Malfunction ·HEALTHTRONICS, INC.·Product code LNS·February 22, 2019

    CARDIOSAVE HYBRID, TYPE G PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·December 31, 2024

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·September 20, 2013

    REFURBISHED PULSAR GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·May 12, 2015

    CARDIOSAVE HYBRID, TYPE G PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 30, 2024

    GENERATOR PULSAR

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·May 12, 2016

    PULSAR GENERATOR REFURBISHED

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·June 3, 2015

    CARDIOSAVE HYBRID, TYPE G PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·June 3, 2024

    HYPERBARIC CHAMBER

    FDA Adverse Event
    Malfunction ·SECHRIST INDUSTRIES, INC.·Product code CBF·March 9, 2017

    CARDIOSAVE HYBRID, TYPE G PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·April 23, 2024

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·October 7, 2016