BEUDAMED
    27 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Zenith Flex System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    COMFORTPRESS VASCULAR COMPRESSION ASSIST DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LO-50 LED LIGHT SOURCE

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

    GMK-REVISION FIXED TIBIAL INSERT SC SIZE 4/17MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 2, 2020

    AORTIC EXCLUDER AAA ENDOPROSTHESIS (LOW PROFILE)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·October 30, 2018

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·April 3, 2020

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 11, 2013

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM

    FDA Adverse Event
    Malfunction ·BIOENTERICS CORP·Product code LTI·September 17, 2008

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·June 15, 2011

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·August 26, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·September 26, 2018

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·February 4, 2020

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·July 9, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·July 3, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·October 12, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·August 7, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·February 11, 2020

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·May 3, 2019

    MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·April 8, 2019

    AORTIC MOLDING AND OCCLUSION BALLOON CATHETER (MOB)

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DQY·February 4, 2020