BEUDAMED
    7,490 results · 36ms · Sources: EU EUDAMED, US FDA

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    OXYCON MOBILE

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code BZC·March 30, 2016

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·June 8, 2007

    VITEK® 2 YEAST (YST) IDENTIFICATION (ID) TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code JXB·February 7, 2017

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO INC·Product code GJS·March 12, 2012

    COAGUCHEK PT TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·April 20, 2005

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·April 5, 2011

    ETHICON

    FDA Adverse Event
    Injury ·C G LABS·Product code GCJ·March 25, 2002

    INRATIO2

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·September 27, 2010

    COBAS INTEGRA 800 ANALYZER

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 30, 2007

    PALAXTREME, R50 VEINED, 1000G

    FDA Adverse Event
    Injury ·KULZER·Product code EBI·September 23, 2020

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·March 10, 2009

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·March 10, 2009

    LIFECODES HLA-B SSO TYPING KIT, LIFECODES HLA-B ERES SSO TYPING KIT

    FDA Adverse Event
    Malfunction ·IMMUCOR GTI DIAGNOSTICS, INC.·Product code MZI·May 24, 2018

    VITEK® 2 GRAM POSITIVE TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code LQL·December 14, 2017

    VITEK® 2 GRAM POSITIVE TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code LQL·December 14, 2017

    VITEK® 2 GP TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LQL·February 1, 2018

    VITEK® 2 GP TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LQL·February 1, 2018

    VITEK® 2 GP TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LQL·February 1, 2018

    STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

    FDA Adverse Event
    Malfunction ·NEURO - VILLABA·Product code LGW·November 14, 2011

    FIBEROPTIX ULTRA 8 LAB--8FR 30CC

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL, LLC (SUBSIDIARY OF TELEFLEX, INCORPORATED)·Product code DSP·August 6, 2024