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

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    GATEWAY ADVANAGE Y-ADAPTER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    D-Fine Double Diamond™ Trial Kit #09

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172001779·Dental burnisher

    Humeral Cup Stability

    FDA UDI
    FX SOLUTIONS·03701037310540·HUMERAL CUP 135/145° STABILITY PE/TA6V Ø36 +9

    Humeral Cup Stability

    FDA UDI
    FX SOLUTIONS·03701037311370·TRIAL HUMERAL CUP 135/145° STABILITY Ø36 +9

    Humeral Cup Stability

    FDA UDI
    FX SOLUTIONS·03701037314074·STABILITY TRIAL HUMERAL CUP CUSTOM MADE 135/145...

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857561335·Angled Box Chisel Size 8 mm

    REPROCESSED COMPRESSION SLEEVES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AAP ACROPLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    WONDFO

    FDA Adverse Event
    Malfunction ·GUANGZHOU WONDFO BIOTECH CO., LTD.·Product code LCX·September 28, 2016

    INSPIRE 7F M N/S

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

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·May 24, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORP.·Product code LGW·August 21, 2008

    INSPIRE 7F M N/S

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

    OSSEOTITE TAPERED CERTAIN PREVAIL IMPLANT 4/3 X 13MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·September 29, 2025

    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