BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    Patient Cables and Leadwires , Disposable ECG Leadwires

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INVOS CEREBRAL/SOMATIC OXIMETER SYSTEM, MODEL: 5100C

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CLEARVISION DR 7000F

    FDA 510(k)
    FDA Class 2 ·Radiology

    MOBILELINK ACETABULAR CUP SYSTEM

    FDA Adverse Event
    Malfunction ·WALDEMAR LINK GMBH & CO. KG·Product code LPH·February 20, 2025

    VACUETTE

    FDA Adverse Event
    Malfunction ·GREINER BIO-ONE GMBH·Product code JKA·July 22, 2011

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 10, 2013

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM

    FDA Adverse Event
    Malfunction ·BIOENTERICS CORPORATION·Product code LTI·September 29, 2008

    SENSATION PLUS 8FR. 50CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·May 10, 2022

    PEN NDL 32G 4MM PRO 100 BOX 1200 US

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMI·July 30, 2021

    SENSATION PLUS 7.5FR. 40CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·February 23, 2021

    BD NANO¿ 2ND GEN PEN NEEDLES 32G X 4MM (100 COUNT)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·October 25, 2023

    BD PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·February 23, 2021

    SENSATION 7FR. 34CC IAB

    FDA Adverse Event
    Death ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·February 2, 2021