BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    CRYO CHECK LOW FIBRINOGEN CONTROL

    FDA 510(k)
    FDA Class 2 ·Hematology

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074321974·DISTRACTOR 8951823 C-STYLE 18MM X 15MM

    UE BRONCHO Single-Use Bronchoscopes (EBS-380C); UE BRONCHO Single-Use Bronchoscopes (EBS-500C); UE BRONCHO Single-Use Bronchoscopes (EBS-600C); UE Display (UE-M10S)

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    DISPOSABLE ISOLATION GOWN

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    ENDO GIA

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code GDW·November 12, 2010

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./ HUNTINGTON·Product code HQL·July 2, 2014

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code KNS·October 21, 2022