BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    COAGULATION REFERENCE PLASMA, NORMAL

    FDA 510(k)
    FDA Class 2 ·Hematology

    BD EMERALD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 23, 2020

    EZ-SCREEN:OPIATES

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HYPODERMIC SYRINGE LUER LOK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTRASAFE X225L PR WHITE SSL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MEG·October 28, 2020

    GARBIN I

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·May 28, 2014

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·January 9, 2013

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JGS·November 22, 2010

    Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 26, 2015