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

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    GYROSCAN INTERA (R7.5)

    FDA 510(k)
    FDA Class 2 ·Radiology

    IPG Medical

    FDA UDI
    IPG Medical Corporation·00810071230943·IPG Medical, Flat Tip, Single-Use Laser Fiber, ...

    5 ML BD LUER-LOK¿ SYRINGE BULK STERILE PHARMACY CONVENIENCE TRAY

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 5, 2017

    5 ML BD LUER-LOK¿ SYRINGE BULK STERILE PHARMACY CONVENIENCE TRAY

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 5, 2017

    MAGIC MOBILITY 4 X 4 WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BURR HOLE COVER, MODEL XX

    FDA 510(k)
    FDA Class 2 ·Neurology

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024371064·Fashion Arm Sling, Medium Box 10

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024371101·Fashion Arm Sling, X-Large Box 10

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024371040·Fashion Arm Sling, Small Box 10

    5 ML BD LUER-LOK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·August 28, 2017

    CARDIOSAVE

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 30, 2013

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 4, 2023

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 21, 2012

    ZOOM CRITICAL CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·February 3, 2011

    ANALYTICAL E MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·February 19, 2008

    CARDIOSAVE

    FDA Adverse Event
    Malfunction ·DATASCOPE MAHWAH·Product code DSP·October 19, 2017

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·May 11, 2023

    CARDIOSAVE HYBRID INTRA-AORTIC PUMP

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 15, 2014

    VUELOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020

    VEULOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020