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

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    AIRPREP SYSTEM - MODEL 9001

    FDA 510(k)
    FDA Class 2 ·Dental

    KALTOSTAT WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    REVISED LABELING FOR TDX CANNABINOIDS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code GWM·January 31, 2017

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code GWM·January 31, 2017

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code GWM·December 16, 2016

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT - 10886704075486

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·April 20, 2016

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT - 10886704075486

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·April 20, 2016

    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

    LIGAMAX-5MM

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 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

    ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT - 10886704075486

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·April 20, 2016