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

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    SILK

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    2993999

    FDA Adverse Event
    Malfunction ·March 1, 2013

    ARP POV SPORT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    OBUTMENT HB

    FDA 510(k)
    FDA Class 2 ·Dental

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 17, 2022

    STERRAD 100S STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·June 8, 2006

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·March 17, 2022

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 16, 2011

    SELECTSECURE MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVN·April 1, 2024

    SELECTSECURE MRI SURESCAN

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code NVN·April 1, 2024

    SELECTSECURE MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVN·April 1, 2024

    UNKNOWN CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·October 14, 2016

    STERRAD 100NX STERILIZER 1-DR

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·January 6, 2021