BEUDAMED
    3,076 results · 31ms · 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 ×

    GPE MedTech Systeme GmbH

    FDA registration
    GPE MedTech Systeme GmbH·9 products·🇩🇪 Germany

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·July 12, 2023

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MFR·September 28, 2016

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·November 7, 2018

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·September 21, 2018

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·July 24, 2013

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MFR·September 28, 2016

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·Product code CAZ·February 26, 2020

    POLY-L-LACTIC ACID (POLY-L-LACTIC ACID)

    FDA Adverse Event
    SANOFIAVENTIS U.S. LLC·Product code LMH·January 5, 2010

    UNKNOWN PRODUCT-PR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code KNT·November 27, 2018

    VERCISE CARTESIA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·April 1, 2024

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·October 3, 2016

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·October 3, 2016

    PORTEX BLUSELECT SUCTIONAID CUFFED TRACHEOSTOMY

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL CZECH REPUBLIC A. S·Product code BTO·December 6, 2024

    SCULPTRA (POLY-L-LACTIC ACID)

    FDA Adverse Event
    Injury ·SANOFIAVENTIS U.S. LLC·Product code LMH·November 15, 2010

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·January 9, 2020

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code BSO·October 24, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code CAZ·October 24, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code BSO·December 13, 2019

    EPIDURAL CATHETERIZATION SET

    FDA Adverse Event
    Malfunction ·Product code CAZ·September 29, 2020