BEUDAMED
    7 results · 28ms · 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.

    ASTRO TRACE (MODEL AT-02)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LARGE AO COUPLING ASNIS III HALL FITTING

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 25, 2012

    CURITY FIBEROPTIC INTUBATING AIRWAY

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    LAPAROFLATOR 3000, STANDARD AND ELECTRONIC

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 19, 2014

    UNKNOWN DEPUY DURALOC 28X54MM +4 10D LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·October 22, 2010

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·December 26, 2012