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

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    MEBBY GENTLEFEED DUO BREAST PUMP/DUAL EXPRESSER PUMP

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

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810057373114·D850 Transfer Board Small Pad

    VITROS IMMUNODIAGNOSTIC PRODUCTS FOLATE RANGE VERIFIERS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SCHOTTLANDER ENIGMA COLOUR TONE, MODEL 0156

    FDA 510(k)
    FDA Class 2 ·Dental

    BD INTIMA-II 24GAX0.75IN PRN SLM NPVC

    FDA Adverse Event
    Malfunction ·BD SUZHOU (MDS)·Product code FOZ·October 8, 2024

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·April 29, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·April 20, 2011

    LEAD MODEL 302

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·July 25, 2008

    BD INTIMA-II

    FDA Adverse Event
    Malfunction ·BD SUZHOU (MDS)·Product code FOZ·August 6, 2024

    BD INTIMA-II 24GAX0.75IN PRN SLM NPVC

    FDA Adverse Event
    Malfunction ·BD SUZHOU (MDS)·Product code FOZ·October 9, 2024

    BD INTIMA-II 24GAX0.75IN PRN SLM NPVC

    FDA Adverse Event
    Malfunction ·BD SUZHOU (MDS)·Product code FOZ·October 21, 2024

    BD INTIMA-II 24GAX0.75IN PRN SLM NPVC

    FDA Adverse Event
    Malfunction ·BD SUZHOU (MDS)·Product code FOZ·October 29, 2024

    BD INTIMA-II 24GAX0.75IN PRN SLM NPVC

    FDA Adverse Event
    Malfunction ·BD SUZHOU (MDS)·Product code FOZ·September 26, 2024

    BLUNT TIP SCREW, 4X36MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·February 3, 2023

    BD INTIMA-II 24GAX0.75IN PRN SLM NPVC

    FDA Adverse Event
    Malfunction ·BD SUZHOU (MDS)·Product code FOZ·October 22, 2024

    BLUNT TIP SCREW, 4X40MM

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code HSB·February 3, 2023

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 10, 2019

    AXIUM

    FDA Adverse Event
    Malfunction ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·October 11, 2019