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

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    BIS

    FDA Adverse Event
    Injury ·COVIDIEN LLC·Product code OLW·April 23, 2026

    SEF-LIFT

    FDA Adverse Event
    Injury ·ARJO, INC.·Product code FSA·July 5, 2005

    RD SEDLINE SENSOR

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code MWI·July 10, 2018

    SEDLINE KIT

    FDA Adverse Event
    Malfunction ·MASIMO - 40 PARKER·Product code MWI·November 6, 2018

    RESTORE 5X10 SEF-TAP+

    FDA Adverse Event
    Injury ·LIFECORE BIOMEDICAL, INC.·Product code DZE·June 28, 1997

    SEF CENT HIP 46X28 BRN

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·January 6, 2010

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·November 19, 2018

    BINAXNOW COVID-19 ANTIGEN SELF TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QKP·April 15, 2022

    ORION SEF IPG 5.3AH TONIC NONRECHARGEABLE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·October 11, 2018

    TACTIFLEX SE F-CURVE ABLATION CATHETER

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code OAE·January 28, 2026

    MICRA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code PNJ·December 9, 2016

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·August 15, 2017

    SPRINT QUATTRO SECURE MRI SURESCAN LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVY·January 9, 2025

    ABC SE;F-LOCKING CERVICAL SCREW 4.0X16MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code KWQ·April 10, 2015

    INSYNC

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWP·December 10, 2014

    CENTROVENA ONE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code SEF·May 27, 2026

    CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Injury ·UNKNOWN·Product code SEF·May 6, 2026

    CENTROVENA ONE

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD) -3006260740·Product code SEF·May 6, 2026

    CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Injury ·UNKNOWN·Product code SEF·May 6, 2026

    CENTROVENA ONE

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code SEF·March 25, 2026