BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    KENDALL MODU-VAC CLOSED SUCTION SYSTEM

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    ALT/GPT REAGENT SET

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NEW TRIAD VLC CROWN & BRIDGE PROVISIONAL MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·September 10, 2021

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·February 5, 2013

    ARIA RADIATION ONC MGT SYS

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS·Product code IYE·December 6, 2010

    BLACKMAX-NEURO

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBB·July 18, 2014

    JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023

    JAWS "HIQ+", 5 X 330 MM, SCISSORS, METZENBAUM

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 30, 2023

    SHAFT "HIQ+", 5 X 330 MM

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·May 23, 2023

    JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023

    ev3 Pipeline Flex Embolization Device. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020