BEUDAMED
    16 results · 41ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NOBELREPLACE TAPERED GROOVY WP 5X8MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE USA, LLC·Product code DZE·October 14, 2019

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·February 9, 2025

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 17, 2024

    RIATA ST OPTIM LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVY·May 10, 2021

    OCTRODE LEAD KIT, 90CM LENGTH

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·October 14, 2021

    OCTRODE LEAD KIT, 90CM LENGTH

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·October 14, 2021

    ZEPHYR XL SR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code NVZ·December 26, 2019

    QUICKFLEX LV LEAD

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code OJX·November 17, 2020

    UNIFY ASSURA CRT-D RF HV

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NIK·November 17, 2020

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVY·November 17, 2020

    DELTA CER HEAD 12/14 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code LZO·May 6, 2017

    MCGHAN

    FDA Adverse Event
    Injury ·MCGHAN MEDICAL·Product code FWM·June 27, 1997

    AUTO SUTURE ENDO GIA II 12MM STAPLER

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GCJ·February 21, 2001

    AUTO SUTURE MULTIFIRE TA 55-4.8

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP.·Product code GAG·March 30, 1999

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 16, 2013

    IMPELLA RP

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code PYX·September 12, 2024