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

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    Zimmer Trabecular Metal Reverse Shoulder System, Mini Glenoid

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUASAR BLUE LIGHT THERAPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CARDIO XP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 6, 2025

    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

    ETRIO

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·July 22, 2011

    OLYMPUS RESECTION SHEATH

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·May 31, 2013

    ACRYSOF TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MJP·September 18, 2008

    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

    BD¿ BLOOD COLLECTION ASSEMBLY WITH MALE LUER LOCK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·November 27, 2018

    BD¿ BLOOD COLLECTION ASSEMBLY WITH MALE LUER LOCK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·October 24, 2018

    BD BLOOD COLLECTION ASSEMBLY WITH MALE LUER LOCK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·November 30, 2018