BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    CARTIVA

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·July 21, 2020

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·December 10, 2018

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·December 10, 2018

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·December 10, 2018

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·August 31, 2018

    PROCLAIM¿ DRG IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·August 5, 2019

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 7, 2014

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·August 19, 2019

    KIT IMPLANTABLE SLIM TIP LEAD, 50CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·August 19, 2019

    CARTIVA DEVICE 10MM T20-0329

    FDA Adverse Event
    Injury ·CARTIVA, INC·Product code PNW·April 23, 2021

    PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE

    FDA Adverse Event
    Injury ·CORCYM S.R.L.·Product code LWR·February 25, 2025

    PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE

    FDA Adverse Event
    Injury ·CORCYM S.R.L.·Product code LWR·January 12, 2025