BEUDAMED
    87 results · 25ms · Sources: EU EUDAMED, US FDA

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    Pangea Platform; Pangea Femur Plating System; Pangea Humerus Plating System; Pangea Tibia Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SITE-RITE NEEDLE GUIDE KITS AND PROBE COVER KIT

    FDA 510(k)
    FDA Class 2 ·Radiology

    PINPOINT GT SAFETY INTRODUCER NEEDLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PSI KIT: 8.5 FR X 4-1/8 (10 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DYB·January 17, 2013

    PSI KIT: 8.5 FR X 4-1/8 (10 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DYB·January 17, 2013

    PSI KIT: 8.5 FR X 4-1/8 (10 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DYB·January 17, 2013

    PSI KIT: 8.5 FR X 4-1/8 (10 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DYB·January 17, 2013

    PSI KIT: 8.5 FR X 4-1/8 (10 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DYB·January 17, 2013

    2242445-2008-00037

    FDA Adverse Event
    Injury ·Product code DYG·October 31, 2008

    2242445-2008-00038

    FDA Adverse Event
    Injury ·Product code GBZ·October 31, 2008

    2242445-1999-00057

    FDA Adverse Event
    Malfunction ·December 21, 1999

    2242445-1999-00056

    FDA Adverse Event
    Malfunction ·December 21, 1999

    2242445-2001-00004

    FDA Adverse Event
    Injury ·Product code DYG·June 12, 2001

    CATH PKGD: BERMAN 5 FR 8 0CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code DQO·February 24, 2011

    CATH PKGD: BERMAN 5 FR 80CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC·Product code DQO·February 24, 2011

    CATH PKGD: BERMAN 5 FR 8 0CM

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DQO·February 24, 2011

    INTRO CHOLANGIOGRAPHY SET

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code FGE·February 6, 2014

    PERCUTANEOUS THROMBOLYTIC DEVICE KIT: 7

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DXE·September 23, 2011

    UNKNOWN PORT

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code LJT·February 1, 2006

    CATH PKGD: THERMISTOR 5.80CM

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DYG·December 20, 2011