BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    SAS BRUCELLA AMS ANTISERUM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    X-spine Pedicle Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO: LIFESTENT VALEO BILIARY STENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LIFESTENT VALEO BILIARY STENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·December 29, 2009

    LIFESTENT VALEO BILIARY STENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·December 29, 2009

    LIFESTENT VALEO VASCULAR STENT

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·August 9, 2010

    VALEO VASCULAR STENT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code FGE·September 3, 2010

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    ENTERALITE INFINITY ENTERAL FEEDING PUMP

    FDA Adverse Event
    Other ·MOOG MEDICAL DEVICES GROUP·Product code LZH·December 29, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 23, 2014

    LIGACLIP ENDOSCOPIC ROTATING MCA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 6, 2017