BEUDAMED
    7 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·TRI-TECH FORENSICS, INC.·Product code JKA·July 29, 2025

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·January 8, 2013

    HT70 VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·January 11, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    WIRELESS BATTERY MODULE G

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 5, 2014