BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    IPOS G.L.P. SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SYNTHES (USA) PATIENT SPECIFIC CRANIAL/CRANIOFACIAL IMPLANTS

    FDA 510(k)
    FDA Class 2 ·Neurology

    ASTRAL VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LONG NAIL KIT R2.0, TI, RIGHT GAMMA3 11X360MM X 1

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code JDS·October 11, 2012

    NO CODE AVAILABLE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code GXN·March 8, 2016

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 27, 2014

    HUDSON CORR-A-FLEX TUBING

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BZO·November 5, 2012

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·September 8, 2010

    PLATE, CRANIOPLASTY, PREFORMED, ALTERABLE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code GWO·June 21, 2016

    dS Breast 7ch 3.0T

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 4, 2024