BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    Reform® POCT System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·24026704511079·

    PERKINELMER XRD 1622 AP3 MED FLAT PANEL DETECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    M3290B INTELLIVUE INFORMATION CENTER SOFTWARE, RELEASE A.0

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INTELLIVUE INFO CENTER IX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·December 19, 2023

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 17, 2013

    TERUMO CDI 540 CALIBRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·June 24, 2011

    TRAPEZOID RX LITHOTRIPTER COMPATIBLE BASKET

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LQC·September 19, 2008

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MHX·March 15, 2023

    ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020

    ZYSTON IMPLANT, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·August 22, 2020