BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    DSL ACTIVE NON-EXTRACTION IGF-I IRMA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    C-STEM

    FDA UDI
    DEPUY (IRELAND)·10603295235279·C-STEM Stem High Offset SIZE 4 9/10 TAPER CEMENTED

    PAJUNK MULTISTIM SENSOR NERVE STIMULATORS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TRIS BUFFERED SALINE

    FDA 510(k)
    FDA Class 2 ·Hematology

    INSPIRA TEXTURE COHESIVE SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·July 6, 2022

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 11, 2016

    AFFINITY THREE BIRTHING BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC·Product code HDD·January 17, 2013

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 15, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 11, 2011

    Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems, Sterile EO, Rx only. Models BVT608010V01, BVT608030V01, BVT612010V01, BVT612030V01, CVT808015, CVT808025, CVT812015, CVT812025, EVT808015, EVT808025, EVT812015, EVT812025, BVT808015, BVT808030, BVT812015, BVT812030, EUT808015, EUT808030, EUT812015, EUT812030. Product Usage: The Trellis 6 and Trellis 8 peripheral infusion system is intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature.

    FDA Enforcement
    Class II ·Terminated·Medtronic Inc. Cardiac Rhythm Disease Management·April 8, 2015