BEUDAMED
    10 results · 17ms · 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 ×

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 8, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 23, 2011

    ACCU-CHEK ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code FPA·May 8, 2008

    TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM SIZE CD 11 MM THICKNESS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBH·August 3, 2018

    TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM SIZE CD 11 MM THICKNESS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBH·August 3, 2018

    TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM SIZE CD 11 MM THICKNESS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBH·August 3, 2018

    TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM SIZE CD 11 MM THICKNESS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBH·August 3, 2018

    TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM SIZE CD 11 MM THICKNESS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBH·August 3, 2018

    TIBIAL ARTICULAR SURFACE PROVISIONAL SHIM SIZE CD 14 MM THICKNESS

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBH·August 2, 2018

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code KPE·August 5, 2011