BEUDAMED
    49 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    AnyRidge Octa 1 Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528127964·2.4 X 48mm Cannulated Headed Screw, T7

    DISPOSABLE VINYL SYNTHETIC EXAMINATION GLOVES, POWDERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PULSIOFLEX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·May 5, 2020

    INSPIRE 8F M

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·January 3, 2024

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 11, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·July 19, 2011

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·September 12, 2008

    INSPIRE 8F M

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·January 4, 2024

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 12, 2026

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 12, 2026

    INSPIRE 8F

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·November 5, 2025

    INSPIRE 8F

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·November 5, 2025

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA·Product code DTZ·December 11, 2025

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 20, 2021

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·September 11, 2020

    INSPIRE 8F M HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·December 23, 2020

    INSPIRE 8F

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code DTZ·July 24, 2025

    INSPIRE 8F M

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·June 7, 2023