BEUDAMED
    32 results · 29ms · Sources: EU EUDAMED, US FDA

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    FORESEE (4C) IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    Oticon

    FDA UDI
    Oticon A/S·05707131260840·RIA, RITE 312 WL CBE

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1671332090·

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code OVD·December 18, 2019

    FUKUDA DENSHI MODEL FF SONIC UF-750XT

    FDA 510(k)
    FDA Class 2 ·Radiology

    VERIGENE RESPIRATORY VIRUS NUCLEIC ACID TEST +(RVNAT+)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CLYDESDALE PTC SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MAX·October 17, 2019

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·January 25, 2023

    INSPIRE 7F M N/S

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·December 29, 2025

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDJ·May 29, 2013

    IN TOUCH ZU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·May 4, 2011

    HYDROTHERMABLATOR PROCEDURE SET

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MNB·August 22, 2008

    INSPIRE 7F M N/S

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA - S.R.L.·Product code DTZ·February 19, 2026

    HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER AND HARDSHELL VENOUS/CAR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·May 10, 2019

    INSPIRE 6F HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code DTZ·March 10, 2017

    INSPIRE 6F HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·August 3, 2022

    INSPIRE 6 HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·February 25, 2022

    INSPIRE 6

    FDA Adverse Event
    Death ·SORIN GROUP ITALIA SRL.·Product code DTZ·July 15, 2024

    INSPIRE 6F M DUAL HOLLOW FIBER OXY W/ INTEGRATED HARDSHELL VENOUS CARDIOTOMY RES

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·October 17, 2018

    INSPIRE 6F DUAL HOLLOW FIBER OXY W/ INTEGRATED HARDSHELL VEN/CARD RES

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·October 24, 2018