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

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    Pitch PaSoft Tissue Reinforcement Device

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

    Sonic

    FDA UDI
    Sbo Hearing A/S·05714464032525·SONIC RADIANT 60 MNR T BL/DG

    Cooley-Derra Anastomosis Clamp 17cm

    FDA UDI
    Geister Medizintechnik GmbH·04057034062258·Cooley-Derra Anastomosis Clamp 17cm

    MEDTRONIOC 7F LAUNCHER BIOPSY GUIDE CATHETER, MODEL LA7RVBB, MEDTRONIC 8F LAUNCHER BIOPSY CATHETER, MODEL LA8RVBB

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VENACURE EVLT NEVERTOUCH PROCEDURE KIT

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

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FRN·November 17, 2008

    ON-Q CATHETER

    FDA Adverse Event
    Injury ·I-FLOW CORP.·Product code MEB·August 12, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 16, 2013

    VITEK® REVEAL¿ SENSOR PANEL

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·June 23, 2025

    VITEK® REVEAL¿ SENSOR PANEL

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·June 24, 2025

    VITEK® REVEAL¿ SENSOR PANEL

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·June 23, 2025

    VITEK® REVEAL¿ SENSOR PANEL

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·June 24, 2025

    VITEK® REVEAL¿ SENSOR PANEL

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·June 24, 2025