BEUDAMED
    8 results · 20ms · 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.

    KINETIC MODEL 700

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

    BBL DIRECTIGEN TEST KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    6MV PORT FILM CAPABILITY OPTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 14, 2015

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 24, 2014

    LAG SCREWDRIVER 380X110MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·November 3, 2010

    OCTROD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 28, 2012

    TFNA HELICAL BLADE 100MM STERILE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·December 7, 2017