BEUDAMED
    13 results · 44ms · 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.

    BIOJECTOR SYRINGE

    FDA Adverse Event
    Malfunction ·BIOJECT, INC.·Product code KZE·April 25, 1997

    BIOJECTOR

    FDA Adverse Event
    Injury ·BIOJECT, INC.·Product code KZE·March 29, 2006

    BIOJECTOR 2000

    FDA Adverse Event
    Injury ·BIOJECT, INC.·Product code KZE·December 6, 2007

    BIOJECTOR 2000

    FDA Adverse Event
    Injury ·BIOJECT, INC.·Product code KZE·June 13, 2006

    BIOJECTOR

    FDA Adverse Event
    Other ·BIOJECT, INC.·Product code KZE·December 11, 2001

    BIOJECTOR

    FDA Adverse Event
    Malfunction ·BIOJECT, INC.·Product code KZE·February 3, 2005

    #3 SYRINGE

    FDA Adverse Event
    Malfunction ·BIOJECT INC.·Product code FMF·October 26, 1999

    COOL CLICK NOZZLE

    FDA Adverse Event
    Other ·BIOJECT, INC.·Product code KZE·April 23, 2002

    #2 SYRINGE

    FDA Adverse Event
    Malfunction ·BIOJECT INC.·Product code KZE·January 28, 1999

    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

    BIOJECTOR 2000

    FDA Adverse Event
    BIOJECT MEDICAL TECHNOLOGIES, INC.·Product code KZE·August 10, 2006

    ALARIS

    FDA Adverse Event
    Malfunction ·BIOTECT INSTRUMENTS ALARIS MEDICAL SYSTEMS, INC·Product code FRN·May 18, 2001