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

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    GenePOC CDiff

    FDA 510(k)
    FDA Class 2 ·Microbiology

    METOXIT CAM-BLANKS

    FDA 510(k)
    FDA Class 2 ·Dental

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PICC SET

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL INC·Product code MEH·July 20, 2011

    COBAS 8000 C701 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·June 17, 2013

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 19, 2008

    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

    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

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·April 26, 2018

    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

    ESTEEM SYNERGY

    FDA Adverse Event
    Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code EZQ·August 17, 2018

    ESTEEM SYNERGY

    FDA Adverse Event
    Malfunction ·CONVATEC DOMINICAN REPUBLIC INC·Product code EZQ·August 17, 2018