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

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    Vital-Port Vascular Access System Power Injectable Port

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·January 7, 2016

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

    VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

    FDA Adverse Event
    Malfunction ·COOK VASCULAR INC·Product code LJT·January 3, 2019

    VITAL-PORT

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code LJT·May 24, 2016

    HHM

    FDA UDI
    Oticon A/S·05707131281104·H160V2, MINIBTE 312 WL 85 CNB HHM

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100202·NEVYAS DRAPE SPECULUM OPEN WIRE

    OXYCODONE ENZYME IMMUNOASSAY AND OXYCODONE CALIBRATORS AND CONTROLS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    AFX SYSTEM

    FDA Adverse Event
    Death ·ENDOLOGIX, INC.·Product code MIH·June 6, 2013

    ARCHITECT HAVAB-M

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code LOL·July 6, 2011

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008