BEUDAMED
    34 results · 24ms · Sources: EU EUDAMED, US FDA

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    OMNI OXYGEN SYSTEM, MODEL 1000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Natus

    FDA UDI
    XLTEK·00382830016438·Natus Quantum Oximeter Adapter Cable

    Clever Choice Comfort EZ

    FDA UDI
    SIMPLE DIAGNOSTICS INC·00898302139319·Insulin Syringe 30G .3cc 5/16"

    VIVID 7 WITH SONOPAC, MODEL FB0008XX

    FDA 510(k)
    FDA Class 2 ·Radiology

    AMS SACRAL COLPOPEXY SLING, MODEL 72403501

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

    BD VACUTAINER® PLUS CITRATE TUBE 2.7ML WITH LIGHT BLUE HEMOGARD CLOSURE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 5, 2017

    BD VACUTAINER® PLUS CITRATE TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 1, 2017

    BD VACUTAINER® PLUS CITRATE TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 6, 2017

    BD VACUTAINER® CITRATE TUBES 4.5 13X75 NA CITRATE (0.105M = 3.2%)

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 10, 2017

    BD VACUTAINER® PLUS CITRATE TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 14, 2017

    BD VACUTAINER® PLUS CITRATE TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 8, 2017

    CITRATE TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 27, 2017

    SHARP HOOK

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code GDG·March 20, 2013

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011

    ACUVUE OASYS

    FDA Adverse Event
    Other ·JOHNSON & JOHNSON·Product code LPL·March 13, 2008

    BD VACUTAINER® BUFFERED SODIUM CITRATE (9NC) BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·May 24, 2019

    METASUL, ALPHA INSERT, II/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·March 15, 2018

    METASUL, ALPHA INSERT, II/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·June 25, 2018

    DURASUL, ALPHA INSERT, KK/36

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZO·March 6, 2018

    DURASUL, ALPHA INSERT, HOODED, MM/28

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·May 22, 2018