BEUDAMED
    6,066 results · 38ms · 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 Regulation: Us FDA ×

    ATRAMAT

    FDA UDI
    Internacional Farmacéutica, S.A. de C.V.·07500142079894·ATRAMAT POLYESTER SURGICAL SUTURE GREEN USP 2-0...

    7200A MICROPROCESSOR VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN BENNETT CORP.·Product code CBK·November 25, 1997

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·Product code MNT·October 6, 2020

    7200 SERIES MICROPROCESSOR VENTILAT

    FDA Adverse Event
    Malfunction ·PURITAN BENNETT CORP.·Product code CBK·June 3, 1999

    HIGH FREQUENCY OSCILLATING VENTILATOR (HFOV)

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code LSZ·February 7, 2016

    SENSORMEDICS

    FDA Adverse Event
    Malfunction ·CAREFUSION 207, INC·Product code LSZ·October 28, 2009

    ARCTIC SUN® 5000

    FDA Adverse Event
    Malfunction ·MEDIVANCE, INC. ¿ 1725056·Product code DWJ·September 15, 2023

    CAREFUSION

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code BTY·January 17, 2015

    CAREFUSION

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code BTY·January 7, 2015

    DENVER ASCITES SHUNT

    FDA Adverse Event
    Malfunction ·DENVER BIOMATERIALS, INC.·Product code KPM·September 12, 1996

    PERITONEAL SHUNT CATHETER

    FDA Adverse Event
    Injury ·DENVER BIOMATERIALS, INC.·Product code KPM·June 11, 1996

    SHUNT DENVER ASCITES DOUBLE VALVE

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KPM·December 18, 2017

    DENVER PAK W/ SINGLE VALVED SHUNT

    FDA Adverse Event
    Injury ·DENVER BIOMEDICAL, INC.·Product code KPM·November 4, 2003

    SHUNT DENVER ASCITES PAK DOUBLE VALVE

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code KPM·October 1, 2014

    APD CATHETER

    FDA Adverse Event
    Injury ·MEDI-TECH, INC.·Product code KPM·February 25, 1994

    KIT, PLEURX PLEURAL CATHETER

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code KPM·April 27, 2007

    SHUNT PAK, 11.5FR DOUBLE-VALVE

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KPM·May 10, 2022

    UNKNOWN STRATA II VALVE/SHUNT

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code KPM·October 2, 2009

    DENVER SHUNT

    FDA Adverse Event
    Injury ·CAREFUSION CORPORATION/DRAINAGE·Product code KPM·February 19, 2013

    ASCITES SHUNT, PERC ACCESS KIT, DOUBLE VALVE

    FDA Adverse Event
    Death ·CARDINAL HEALTH·Product code KPM·October 10, 2008