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

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    Filters Status: Malfunction ×

    9550 HEART RATE/RESPIRATION MONITOR

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

    LP6+ VOLUME VENTILATOR

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

    ACCU-CHEK ADVANTAGE TEST STRIPS

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

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code JTC·December 20, 1999

    DATASCOPE

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. CARDIAC ASSIST·Product code DSP·March 4, 1999

    CA 210 DIALYZER (CELLULOSE ACETATE)

    FDA Adverse Event
    Malfunction ·NISSHO·Product code FJI·February 21, 2000

    CLINICATH PERIPHERALLY INSERTED CATHETER

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD (FORMERLY DELTEC, INC.)·Product code LJS·February 6, 2004

    CIRCLE "C" DUAL LUMEN CATHETER KIT

    FDA Adverse Event
    Malfunction ·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MED PRODUCTS INC.·Product code KOC·March 10, 1999

    ANGIO-SEAL

    FDA Adverse Event
    Malfunction ·DAIG, A ST. JUDE MEDICAL CO·Product code MGB·May 21, 1999

    STERRAD 100S STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·June 8, 2006

    ENDOPATH THORACIC ENDOSCOPIC LINEAR CUTTER WITH SAFETY

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY·Product code GAG·April 21, 1999

    CADD-PRIZM PCS AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD·Product code MEA·May 28, 2004

    INAHARA-PRUITT CAROTID SHUNT

    FDA Adverse Event
    Malfunction ·HORIZON MEDICAL PRODUCTS, INC.·Product code DQR·March 8, 1999

    CLINICATH PERIPHERALLY INSERTED CATHETER

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD (FORMERLY DELTEC, INC.)·Product code LJS·February 6, 2004

    LIFEPORT INFUSION SET WITH Y-SITE

    FDA Adverse Event
    Malfunction ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·December 6, 1999