BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    Reusable Blood Pressure Cuff, Disposable Blood Pressure Cuff

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEARTWAY POWER MOBILITY SCOOTER, MODEL PT7

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    AP-1010 AND AP-1020 BLOOD GLUCOSE MONITORING SYSTEM, MAJOR GLUCOSE CONTROL SOLUTION

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 23, 2011

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 30, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 19, 2008

    BINAXNOW COVID-19 ANTIGEN SELF TEST OTC

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·June 3, 2022

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 15, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·June 28, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·March 5, 2021