BEUDAMED
    10 results · 37ms · Sources: EU EUDAMED, US FDA

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    The ICHOR Panacea Vascular Embolectomy Catheter System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX

    FDA 510(k)
    FDA Class 2 ·Dental

    LO-50 LED LIGHT SOURCE

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

    1688 AIM 4K CAMERA HEAD WITH INTEGRATED COUPLER - INTERNATIONAL KIT

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·September 13, 2024

    EPOC BGEM TEST CARD

    FDA Adverse Event
    Malfunction ·EPOCAL INC.·Product code CHL·July 6, 2011

    QC+F/PINS Ø1.5-4

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEY·October 17, 2014

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL -NEUROMODULATION·Product code GZB·June 14, 2013

    EMBOSHIELD NAV6 EMBOLIC PROTECTION SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NTE·July 28, 2011

    OT ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·July 7, 2006

    Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)

    FDA Enforcement
    Class II ·Ongoing·Medtronic Inc.·November 29, 2017