BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    FLASH DENT

    FDA 510(k)
    FDA Class 2 ·Dental

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515240506·Ferris Smith Sewall Orbit Ret, 69mmx13mm, no slot

    IBC FLOPUMP WITH GBS COATING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THE POWERWAND SAFETY INTRODUCER WITH AN EXTENDED DWELL CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 24, 2014

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 28, 2013

    UNKNOWN DEPUY BONE CEMENT

    FDA Adverse Event
    Injury ·DEPUY CMW·Product code LOD·December 15, 2010

    M2A TAPER 37/28MM LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 22, 2016

    M2A MODULAR HEAD COMPONENT 28 MM HEAD DIAMETER MINUS 6 MM NECK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 22, 2016