BEUDAMED
    2,771 results · 36ms · Sources: EU EUDAMED, US FDA

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    NEEDLE CLIPPING DEVICE SAFE CLIP

    FDA Adverse Event
    Malfunction ·HDQ PARSIPPANY·Product code FMI·February 23, 2024

    UNKNOWN

    FDA Adverse Event
    Malfunction ·HDQ PARSIPPANY·Product code MMK·February 5, 2024

    SHARPS COLL 1.4L YELLOW TRAY SIZE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MMK·February 17, 2021

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·February 23, 2026

    BD ALARIS SMARTSITE GRAVITY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FPA·December 8, 2025

    BD ALARIS SMARTSITE GRAVITY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FPA·December 8, 2025

    SHARPS COLL CHEMO 3GAL YELLOW NEW CAP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·April 26, 2021

    SHARPS COLL AUS 1.4L YELLOW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code MMK·March 3, 2021

    TEGO¿ CONNECTOR

    FDA Adverse Event
    Injury ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·February 19, 2025

    HEGAR DILATOR

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code HDQ·December 16, 2009

    DILATOR, UTERINE, HANK, D/E, 15/16 FR

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES, LP·Product code HDQ·September 11, 2025

    HANKS UTER DILATOR 11/12

    FDA Adverse Event
    Other ·CODMAN & SHURTLEFF, INC.·Product code HDQ·June 1, 2006

    *

    FDA Adverse Event
    Malfunction ·CODMAN·Product code HDQ·May 2, 2006

    UNK

    FDA Adverse Event
    Other ·UNK·Product code HDQ·February 24, 2000

    COMFORT-FLEX

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HDQ·September 23, 2009

    HEGAR UTERINE DILATOR, DOUBLE-ENDED, 7 1/2", SIZES

    FDA Adverse Event
    Malfunction ·UNK·Product code HDQ·July 26, 2007

    HANK DILATORS 9/10 -19/20 AMERICAN SCALE

    FDA Adverse Event
    Malfunction ·AESCULAP INC·Product code HDQ·March 21, 2018

    HEGAR

    FDA Adverse Event
    Injury ·MILTEX INSTRUMENT CO. INC.·Product code HDQ·July 29, 1999

    DEVICE 1 - MILTEX

    FDA Adverse Event
    Injury ·MILTEX INSTRUMENT CO. INC.·Product code HDQ·July 29, 1999

    HANK DILATOR

    FDA Adverse Event
    Malfunction ·JARRET·Product code HDQ·July 7, 2006