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

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    ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LUMINOS LOTUS MAX

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHINEERS AG·Product code OWB·March 5, 2025

    Luminos dRF Max, Luminos Agile Max, Uroskop Omnia Max, Multitom Rax

    FDA 510(k)
    FDA Class 2 ·Radiology

    NIDEK DC-3000 DIODE LASER PHOTOCOAGULATOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 19, 2013

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·January 18, 2011

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 1, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·September 24, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 26, 2015

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 5, 2015