BEUDAMED
    20 results · 29ms · Sources: EU EUDAMED, US FDA

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    HARDYDISK NORFLOXACIN, 10MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    COUNTERBORE FOR SS SUBMERGED SCREW PLANT

    FDA 510(k)
    FDA Class 2 ·Dental

    CATH-FINDER(TM) CATHETER TRACKING SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIV.·Product code DQY·July 10, 2009

    EXCELSIOR SL-10 PRE-SHAPED 45 CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQO·December 12, 2007

    EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIV·Product code DQO·April 25, 2007

    EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQO·November 14, 2007

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORPORATION·Product code DQO·May 1, 2007

    EXCELSIOR SL-10 PRE-SHAPED CATHETER

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQO·September 14, 2006

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIV OF BOSTON SCIENTIFIC CORP·Product code DQO·January 3, 2007

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQO·September 15, 2006

    EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHER

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code DQO·January 3, 2007

    EXCELSIOR SL-10 PRE-SHAPED J MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code DQO·August 17, 2007

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 13, 2013

    POLARIS SURGICAL LIGHT

    FDA Adverse Event
    Injury ·STERIS CORPORATION - MONTGOMERY·Product code FTD·February 16, 2011

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code FPA·August 8, 2014

    5MM X 73MM CLEAR FLEXIBLE CANNULA THREADED

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code NBH·December 11, 2019

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIV OF BOSTON SCIENTIFIC CORP·Product code DQO·September 14, 2006

    EXCELSIOR 1018 MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP, NEUROVASCULAR·Product code FOZ·August 2, 2006

    Allura Xper FD10; Model Number: 722003;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·January 21, 2026