BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    LOSPA IS ACP System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ECHO VIEW/SHIMASONIC DIAGNOSTIC ULTRASOUND SYSTEM, MODEL SARANO

    FDA 510(k)
    FDA Class 2 ·Radiology

    AG THERMOGRAPHIC CAMERA, MODEL ATIR-M301

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 14, 2017

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 8, 2017

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·July 14, 2011

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 23, 2014

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 10, 2017

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022