BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Reprocessed Supreme Diagnostic Electrophysiology Catheters

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Oncology EDR2 Film

    FDA UDI
    CARESTREAM HEALTH, INC.·40889971161761·ONCO EDR2 FILM 35X43-14X17 RDYPK 50SH

    E.P.T. CERTAINTY 1-STEP PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    EPISIL

    FDA 510(k)
    FDA Unclassified ·Unknown

    REVEAL LINQ

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code DSI·October 10, 2014

    IMPAX CV REPORTING

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

    MODEL NOT SPECIFIED

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·July 8, 2011

    LUCAS 3 CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Death ·JOLIFE AB - 3005445717·Product code DRM·February 6, 2024

    LUCAS 3 CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Death ·JOLIFE AB - 3005445717·Product code DRM·February 6, 2024