BEUDAMED
    19 results · 43ms · Sources: EU EUDAMED, US FDA

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    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

    COBAS® EGFR MUTATION TEST V2 P150044

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·April 1, 2026

    COBAS® EGFR MUTATION TEST V2 P150044

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·April 15, 2026

    COBAS® EGFR MUTATION TEST V2 P150044

    FDA Adverse Event
    Malfunction ·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code OWD·March 27, 2025

    MONOPOLAR CURVED SHEARS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 6, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 5, 2011

    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 SUTURELESS AORTIC HEART VALVE

    FDA Adverse Event
    Death ·CORCYM S.R.L.·Product code LWR·April 10, 2025

    PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE

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

    PERCEVAL PLUS SUTURELESS AORTIC HEART VALVE

    FDA Adverse Event
    Malfunction ·CORCYM S.R.L.·Product code LWR·March 27, 2025

    PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE

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