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

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    Nexiva™ Closed IV Catheter System with NearPort™ IV Access

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116022441·600 micron core/730 micron OD Luer Lock Diode L...

    Vinyl Patient Examination Gloves

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NuEra Tight Family, EMS Model

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OYC·July 5, 2019

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·June 14, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 22, 2024

    FREESTYLE LIBRE 2 PLUS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code QBJ·April 7, 2026

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·January 10, 2025

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·November 13, 2008

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·July 22, 2011

    6.0MM TI MATRIX POLYAXIAL SCREW 45MM THREAD LENGTH

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·July 17, 2013

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·August 24, 2017

    UNSPECIFIED BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·October 15, 2025

    BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE 5MG/4MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·May 23, 2024

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·October 24, 2017

    PRODIGY AUTOCODE

    FDA Adverse Event
    Malfunction ·OK BIOTECH CO., LTD.·Product code NBW·July 13, 2017

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·June 20, 2017

    BONE PLATE

    FDA Adverse Event
    Injury ·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code JEY·January 8, 2018

    VYPRO MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·March 24, 2022