BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    CHASE ANASTOMOSIS VISUALIZATION DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EMIT(R) II CANNABINOID 100 NG ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PSO KNEE BONE SUBSTITUTION

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRO·April 22, 2022

    PSO KNEE BONE SUBSTITUTION

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRO·July 18, 2019

    ENTERALITE INFINITY ENTERAL FEEDING PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code LZH·January 29, 2013

    PRECISION TEST STRIPS

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

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014

    UNKNOWN HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 16, 2018

    IRC2100 W/ 210 LIGHTGUIDE

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code KNS·August 28, 2019