BEUDAMED
    10 results · 51ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    JETSTREAM G3

    FDA Adverse Event
    Injury ·PATHWAY MED TECHNOLOGIES, INC.·Product code MCW·December 29, 2010

    SIMON NITINOL VENA CAVA FILTER

    FDA Adverse Event
    Injury ·NITINOL MED TECHNOLOGIES, INC.·Product code DTK·January 10, 1995

    BIOJECTOR B2000

    FDA Adverse Event
    Other ·BIOJECT MED TECHNOLOGIES, INC·Product code KZE·January 8, 2007

    BIOJECTOR B2000

    FDA Adverse Event
    Other ·BIOJECT MED TECHNOLOGIES, INC·Product code KZE·January 9, 2007

    CALYPSO BEACON TRANSPONDERS

    FDA Adverse Event
    Injury ·CALYPSO MED TECHNOLOGIES INC·Product code IYE·January 12, 2010

    SUBCLAVIAN CATHETER

    FDA Adverse Event
    Malfunction ·NEOSTAR MED TECHNOLOGIES, INC.·Product code LFJ·August 28, 1995

    SAFETRACE TX

    FDA Adverse Event
    Malfunction ·GLOBAL MED TECHNOLOGIES, INC./WYNDGATE TECHNOLOGIES DIV·Product code MMH·October 11, 2001

    SAFETRACE

    FDA Adverse Event
    Malfunction ·WYNDGATE TECHNOLOGIES / DIV GLOBAL MED TECHNOLOGIES, INC.·Product code MMH·February 28, 2001

    SAFETRACE

    FDA Adverse Event
    Malfunction ·WYNDGATE TECHNOLOGIES DIVISION/GLOBAL MED TECHNOLOGIES, INC.·Product code MMH·July 22, 1999

    SAFETRACE

    FDA Adverse Event
    Malfunction ·WYNDGATE TECHNOLOGIES DIVISION GLOBAL MED TECHNOLOGIES, INC·Product code MMH·March 8, 1999