BEUDAMED
    6 results · 18ms · 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.

    OTT CERVICAL TENACULUM

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

    SCIMEDX PHASE II PR3 IGG ANTIBODY EIA

    FDA 510(k)
    FDA Class 2 ·Immunology

    PHILIPS ECG LEADWIRE SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WIDE SPACED QUATTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 18, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 2, 2014

    PRIME BIG WHEEL STRETCHER 26"

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·December 19, 2012