BEUDAMED
    9 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.
    Filters Regulation: Us FDA ×

    COE PAK AUTO MIX, REGULAR OR HARD SET

    FDA 510(k)
    FDA Class 2 ·Dental

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517310880·Archon Screw, 4.0x22mm S.T. Variable

    X-Box

    FDA UDI
    INNO Holdings, Inc.·M71188814220·PEEK, Ta

    SPRINT Peripheral Nerve Stimulation System, Extensa, SPRINT Peripheral Nerve Stimulation System, Endura, SPRINT Clinical Programmer Kit

    FDA 510(k)
    FDA Class 2 ·Neurology

    KWIK-FLO URINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SROM*STM ST,36+8L NK,22X17X165

    FDA Adverse Event
    Injury ·DEPUY IRELAND·Product code JDI·April 2, 2012

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·May 12, 2014

    REPLACEMENT BULB FOR X7000 (300 WATTS)

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·October 19, 2010

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·December 17, 2012