BEUDAMED
    135 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    SPECTRANETICS GLIDELIGHT LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS·Product code MFA·December 1, 2016

    SPECTRANETICS LASER SHEATH II

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·January 3, 2012

    SPECTRANETICS LASER SHEATH II

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·January 5, 2012

    SPNC LASER SHEATH/LEAD LOCKING DEVICE

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·March 9, 2010

    SPNC LASER SHEATH/LEAD LOCKING DEVICE

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·March 9, 2010

    SPNC LASER SHEATH/LEAD LOCKING DEVICE

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·March 12, 2010

    SPECTRANETICS LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·March 9, 2010

    SPNC LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·January 8, 2010

    SPECTRANETICS LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·June 30, 2010

    SPNC LASER SHEATH/LEAD LOCKING DEVICE

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·May 17, 2010

    SPECTRANETICS LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·June 30, 2010

    SPECTRANETICS LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·June 30, 2010

    SPNC LASER SHEATH/LEAD LOCKING DEVICE

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·May 20, 2010

    SPNC LASER SHEATH/LEAD LOCKING DEVICE

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·May 26, 2010

    SPECTRANETICS LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·June 30, 2010

    SPECTRANETICS LASER SHEATH II

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·April 11, 2012

    LEAD LOCKING DEVICE #1

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code DRB·April 11, 2012

    THROMCAT XT THROMECTOMY CATHETER

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MCW·December 2, 2010

    THROMCAT THROMECTOMY CATHETER

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MCW·December 2, 2010

    SPECTRANETICS LASER SHEATH II

    FDA Adverse Event
    Injury ·SPECTRANETICS CORP.·Product code MFA·October 6, 2010