BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SureFlo EVD Catheter

    FDA 510(k)
    FDA Class 2 ·Neurology

    CAS FIXATION PIN 3.2 DIA X 180 MM STR, CAS FIXATON PIN 3.2 DIA X 80 MM STR, CAS FIXATON PIN 3.2 DIA X 150 MM

    FDA 510(k)
    FDA Class 2 ·Neurology

    CUSTOMIZED SOUND THERAPY (CST)

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

    GALAXY G3 MINI 1MM X 1CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·August 13, 2020

    I-STAT CHEM8+ CARTRIDGE (SEE H10 FOR EC8+)

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 7, 2017

    BELLAVISTA

    FDA Adverse Event
    Injury ·VYAIRE MEDICAL·Product code CBK·October 14, 2024

    UNK

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·June 14, 2013

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 21, 2011

    NDI PASSIVE SPHERES

    FDA Adverse Event
    Malfunction ·NORTHERN DIGITAL, INC.·Product code HAW·July 11, 2014