BEUDAMED
    9 results · 25ms · 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.

    SIMS CPAP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    3M™ Victory Series™

    FDA UDI
    3M UNITEK CORPORATION·00652221117328·3M™ Victory Series™ First Molar Bands, 953-485,...

    ENROUTE Transcarotid Neuroprotection System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THERATRON EQUINOX, MODELS 80 CM AND 100 CM

    FDA 510(k)
    FDA Class 2 ·Radiology

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 13, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    ECHELON*FLEX60 ARTICULATING

    FDA Adverse Event
    Injury ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GDW·January 10, 2011

    1.5MM SYSTEM 4 HOLE LONG STRAIGHT PLATE

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·December 12, 2017

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·April 14, 2015