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

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    PENTAX EPK-I5010 VIDEO PROCESSOR

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·14026704624406·RUSCH Color Coded Guedel Airway Length 70mm Tra...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L122470120·12mm H x 24mm W x 70mm L XLIF Trial 12 degree L...

    LUGASURE CURVED, SMALL JAW, OPEN SEALER/DIVIDER

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

    PORTA SOLDER 1080 W

    FDA 510(k)
    FDA Class 2 ·Dental

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020

    LIGASURE

    FDA Adverse Event
    Injury ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 16, 2019

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 24, 2020

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·March 14, 2019

    LIGASURE

    FDA Adverse Event
    Malfunction ·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 16, 2021

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 2, 2013

    GLENOID, PE WITH PEG, LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·September 26, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 13, 2011