BEUDAMED
    79 results · 24ms · 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 ×

    MJ7 "VISION" TEST DEVICE

    FDA Adverse Event
    Other ·MEDI-JECT CORP.·Product code KZE·October 5, 1999

    INTEGRA ARTIFICIAL SKIN

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORP.·Product code MGR·August 6, 1999

    ETHICON INC., JOHNSON & JOHNSON

    FDA Adverse Event
    Injury ·*·Product code GAM·March 23, 2000

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    9550 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·August 6, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    MEDTRONIC

    FDA Adverse Event
    Injury ·MEDTRONIC INC·Product code DTB·October 14, 2002

    LP6+ VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·October 4, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·August 6, 1999

    SYNTHES

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code HTW·January 19, 1999

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·October 8, 1999

    LP6+ VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·April 27, 1999

    LP6+ VOLUME VENTILATOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code CBK·August 6, 1999

    PREMICATH

    FDA Adverse Event
    Death ·VYGON GMBH & CO KG·Product code DQO·February 29, 2000

    CIRCLE C SILICONE CATHETER KIT

    FDA Adverse Event
    Other ·HORIZON MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code LFJ·September 28, 1999

    ACCU-CHEK ADVANTAGE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CFR·December 14, 2005

    WILLIAM HARVEY

    FDA Adverse Event
    Injury ·C.R. BARD, INC.·Product code DWF·May 28, 1999

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC.·Product code HQL·March 10, 2000

    VORTEX-AC WITH KIT

    FDA Adverse Event
    Other ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·November 23, 1999