BEUDAMED
    4 results · 15ms · 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 Status: Malfunction ×

    OMNISPAN MENISCAL REPAIR 27DEG

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·June 25, 2020

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 19, 2011

    OMNISPAN MENISCAL REPAIR 27DEG

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·May 20, 2021