BEUDAMED
    9 results · 25ms · 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 FDA Adverse Event ×

    UNK

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017

    UNK

    FDA Adverse Event
    Death ·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017

    UNK

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017

    BRK¿ XS TRANSSEPTAL NEEDLE, 71 CM LENGTH

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code DRC·July 27, 2023

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·April 10, 2013

    CAPSURE SP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·May 8, 2008

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 1, 2011

    PRESTIGE(TM) CERVICAL DISC SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code MJO·February 25, 2019

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code MJO·January 28, 2020