BEUDAMED
    21 results · 91ms · Sources: EU EUDAMED, US FDA

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    FDA UDI
    S-CONNECT CO.,LTD·08800068200020·

    My Yodoc

    FDA UDI
    S-CONNECT CO.,LTD·08800068200006·

    FUKUDA DENSHI MODEL DS-5700 CENTRAL STATION

    FDA Adverse Event
    Malfunction ·FUKUDA DENSHI CO., LTD.·Product code DSI·December 15, 2004

    EVIS EXERA II DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·February 22, 2021

    LUNA G3 BPAP 30VT

    FDA Adverse Event
    Injury ·BMC MEDICAL CO., LTD·Product code BZD·February 11, 2026

    BD MAXPLUS NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 1, 2022

    BD MAXPLUS NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·May 31, 2022

    HD CAMERA HEAD

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·January 3, 2024

    Q-SYTE

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·January 7, 2026

    MALE-FEMALE L.LOCK CAP - ORANGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·July 7, 2021

    OM-10000

    FDA Adverse Event
    Malfunction ·MAQUET (SUZHOU) CO.,LTD.·Product code MWS·January 8, 2020

    GLIDEPATH® LONG-TERM HEMODIALYSIS CATHETER

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code MSD·May 8, 2019

    MAXZERO NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FPA·January 28, 2026

    BURETTE SETS 150 ML.

    FDA Adverse Event
    Malfunction ·Product code FPA·July 28, 2021

    TURBO-JECT SINGLE LUMEN PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·February 11, 2021

    TURBO-JECT SINGLE LUMEN POWER-INJECTABLE PICC

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·February 11, 2021

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code HBC·March 26, 2018

    TURBO-JECT SINGLE LUMEN PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·February 11, 2021

    ASAHI SION BLUE

    FDA Adverse Event
    Malfunction ·ASAHI INTECC CO., LTD.·Product code DQX·July 29, 2024

    GORE® CARDIOFORM ASD OCCLUDER

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MLV·November 13, 2023