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

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    Livia

    FDA 510(k)
    FDA Class 2 ·Neurology

    VOYAGER NC CORONARY DILATATION CATHETER AND NC TREK RX CORONARY DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NOVAPACS

    FDA 510(k)
    FDA Class 2 ·Radiology

    WAVEWRITER ALPHA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 7, 2021

    LOGIC TIBIA PS MOD INSRT SZ 2 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 18, 2024

    NC TREK CORONARY DILATATION CATHETER

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code LOX·December 16, 2022

    ASR 300 SPIKED CUP SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·July 8, 2011

    UNKNOWN DEPUY CERAMIC HEAD

    FDA Adverse Event
    Injury ·DEPUY IRELAND ¿ REG. # 9616671·Product code KXA·June 11, 2013

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014