BEUDAMED
    151 results · 22ms · Sources: EU EUDAMED, US FDA

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    TERUMO SURFLO I.V. CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Lippy

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490034647·PROSTHESIS 1133280 LIPPY CUP PSTN .4X4.0

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517565341·CoRoent Ant TLIF PEEK, 13x13x28mm 0°

    N/A

    FDA UDI
    MEDTRONIC XOMED, INC.·00763000035242·PROSTHESIS 1133280 LIPPY CUP PSTN .4X4.0

    BHDENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    DISCOVERY ELBOW-MOSAIC DISTAL HUMERAL REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONE TOUCH ULTRASMART

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·January 14, 2005

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 1, 2014

    3.5MM 90-S SERFAS ENERGY SUCTION PROBE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GEI·May 29, 2013

    ION PACLITAXEL-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·June 20, 2011

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·October 15, 2024

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 19, 2021

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 22, 2020

    CAPIOX FX05

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·April 21, 2020

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·August 1, 2022

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·November 16, 2022

    CAPIOX FX25 OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·November 17, 2023

    CAPIOX FX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·March 1, 2022