BEUDAMED
    35 results · 24ms · Sources: EU EUDAMED, US FDA

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    OPACIDEN SOLUTION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496070627·BE YOU TONIC, SIZE ML, CHAMPAGNE, GRADUATED COM...

    LifeBand® Load-distributing Band

    FDA UDI
    Zoll Circulation, Inc.·10849111001790·Single-use chest compression band. (3 per pack...

    BD INSULIN SYRINGE W/ BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·August 8, 2019

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SCANDINAVIAN IVF SCIENCES AB, HYBASE-1

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SYRINGE 0.3ML 31GA 6MM HALFUNIT

    FDA Adverse Event
    Injury ·BD MEDICAL - DIABETES CARE·Product code FMF·May 1, 2020

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 11, 2012

    BD INSULIN SYRINGE WITH BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 10, 2020

    BD SYRINGE 0.3ML 31GA 6MM HALFUNIT

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·December 19, 2019

    E-CAM COINCIDENCE MODE [510 (K) K970627)

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC., NMG GROUP·Product code IYX·April 20, 2001

    ASR ACETABULAR CUPS 48

    FDA Adverse Event
    Injury ·DEPUY INTL, LTD.·Product code KWA·December 29, 2010

    CANNULATED CRUCIFORM SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code HXX·April 22, 2013

    FLOSEAL HEMOSTATIC MATRIX

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - HAYWARD·Product code LMF·April 27, 2011

    ADV BASIC SYSTEM, UC/MOB, DOM

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code DXT·July 1, 2008

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 21, 2013

    ASR ACETABULAR CUPS 60

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·October 24, 2015

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·August 21, 2013

    ASR UNI FEMORAL IMPL SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 22, 2013

    ADAPTER SLEEVES 12/14 +8

    FDA Adverse Event
    Injury ·DEPUY INTL.,LTD 8010379·Product code KWA·November 4, 2015