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

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    COBAS CT/NG V2.0 TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    HHM

    FDA UDI
    Oticon A/S·05707131256324·H160, MINIBTE 312 WL 85 SGR HHM

    BD NANO¿ 2ND GEN PEN NEEDLES 4MM X 32G

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·February 2, 2022

    ENVITEC REUSABLE SPO2 SENSORS TYPE NIHON-KOHDEN

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCUMED WRIST AUTOMATIC BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FUJIFILM 600 SERIES ENDOSCOPE EC-600WM

    FDA Adverse Event
    Malfunction ·FUJIFILM CORPORATION·Product code FDF·January 22, 2025

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 1, 2014

    ASR ACETABULAR CUP 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 29, 2013

    ADVIA CENTAUR HBSAG ASSAY

    FDA Adverse Event
    SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code LOM·June 17, 2011

    IMPL TAPERED SCR-V SBM 4. 7MM 4.5MM 16MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·February 10, 2022

    EASYPUMP:LT 270-132: 270 ML, 22ML/HR

    FDA Adverse Event
    Malfunction ·I-FLOW LLC·Product code MEB·November 7, 2014

    BD NANO¿ 2ND GEN PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·May 19, 2022

    EASYPUMP: LT 270-132:270 ML, 22ML/HR

    FDA Adverse Event
    Malfunction ·I-FLOW LLC·Product code MEB·November 7, 2014

    EASYPUMP: LT 270-132: 270 ML, 22ML/HR

    FDA Adverse Event
    Malfunction ·I-FLOW LLC·Product code MEB·November 7, 2014

    EASYPUMP: LT 270-132: 270 ML, 2ML/HR

    FDA Adverse Event
    Malfunction ·I-FLOW CORP.·Product code MEB·February 27, 2014

    LT 270-132: 270 ML, 2 ML/HR

    FDA Adverse Event
    Malfunction ·I-FLOW·Product code MEB·November 7, 2012

    Tapered Screw-Vent Implant, MTX, 4.7mm x 11.5mm, 4.5mm Platform. Catalog Number TSVWB11, Lot 62470008. Class II, 510(k) K13227.

    FDA Recall
    Terminated ·Zimmer Dental Inc·Product code DZE·January 6, 2014

    EASYPUMP: LT 270-132: 270 ML, 22 ML/HR

    FDA Adverse Event
    Malfunction ·I-FLOW LLC·Product code MEB·November 7, 2014

    EASYPUMP LT 270-132: 270 ML, 2 ML/HR

    FDA Adverse Event
    Malfunction ·HALYARD·Product code MEB·March 2, 2015

    EASYPUMP: LT 270-132: 270 ML, 2 ML/HR

    FDA Adverse Event
    Injury ·I-FLOW, LLC·Product code MEB·October 3, 2013