BEUDAMED
    68 results · 17ms · Sources: EU EUDAMED, US FDA

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    PCA PUMP (HOSPIRA LIFECARE PCA)

    FDA Adverse Event
    Other ·HOSPIRA·Product code MEA·July 24, 2014

    SERVO VENTILATOR

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SYSTEMS, INC.·Product code CBK·August 25, 1999

    8.0MM CN RAE FLEX

    FDA Adverse Event
    Other ·MALLINCKRODT MEDICAL·Product code BTR·January 16, 1998

    7.0MM CN RAE FLEX

    FDA Adverse Event
    Other ·MALLINCKRODT MEDICAL·Product code BTR·January 16, 1998

    SOLCOTRANS PLUS

    FDA Adverse Event
    Other ·DAVOL BLOOD MGMT PRODUCTS·Product code CAC·March 16, 1995

    SOLCOTRANS PLUS

    FDA Adverse Event
    Other ·DAVOL BLOOD MGMT PRODUCTS·Product code CAC·July 19, 1995

    INTELLIGENT PUMP

    FDA Adverse Event
    Other ·MCGAW, INC.·Product code FRN·February 11, 1994

    BAXTER PTFE VASCULAR GRAFT

    FDA Adverse Event
    Other ·EDWARDS CVS DIV. BAXTER HEALTHCARE CORP.·Product code DSY·July 8, 1996

    MEDICAL SPECIALTIES DIST. INC

    FDA Adverse Event
    Other ·MEDICAL SPECIATIES DISTRIBUTORS, INC.·Product code FPA·June 27, 2005

    HOSPIRA

    FDA Adverse Event
    Other ·HOSPIRA, INC.·Product code FRN·January 3, 2007

    ESSURE

    FDA Adverse Event
    Other ·CONCEPTUS·Product code HHS·August 2, 2011

    TRAVENOL

    FDA Adverse Event
    Other ·BAXTER·Product code FRN·January 14, 2008

    EASYPUMP

    FDA Adverse Event
    Other ·I-FLOW CORP.·Product code MEB·September 23, 2010

    DIALINES

    FDA Adverse Event
    Other ·B. BRAUN MEDICAL, INC.·Product code FJK·December 10, 1999

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ IMAGING·Product code FWG·March 22, 2008

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Other ·GAMBRO LUNDIA AB, MONITOR DIV.·Product code FII·August 18, 2006

    OUTLOOK 200

    FDA Adverse Event
    Other ·B. BRAUN MEDICAL, INC.·Product code FRN·November 1, 2006

    ASIC MSIII MULTI CHANNEL INFUSION PUMP

    FDA Adverse Event
    Other ·ALARIS MEDICAL SYSTEMS·Product code FRN·November 8, 2002

    BIO-SUTURE TAK WITH NEEDLE, 3.0MM

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MAI·July 21, 2004

    *

    FDA Adverse Event
    Other ·*·Product code MQS·May 24, 2006