BEUDAMED
    115 results · 35ms · Sources: EU EUDAMED, US FDA

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    ENDEAVOUR MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Preat

    FDA UDI
    Preat Corporation·00842092169957·Preci Post Reamers (2-Pack)

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694055154·PrimaLIF Plastic Depth Probe

    Mini Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746108471·DB BKT MINI MS UL LAT 018 T+18 A+6 R=0

    Tubing Cartridge Set, M3000, Pack 4

    FDA UDI
    Medical Technical Products, Inc.·00850039020292·

    Alliant Biotech

    FDA UDI
    MEDISURGE LLC·G6112201020040·Symmetric Total Knee Femoral Component Size 4 Left

    Symmetric TK Femoral Component

    FDA UDI
    SIGNAL MEDICAL CORPORATION·B0462201020040·4LT Symmetric TK Femoral Component

    EASY GUIDE ELECTROSURGICAL ACCESS DEVICE

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

    ZYBIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    V200 / ESPRIT

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 16, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 28, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 19, 2021

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code CBK·May 20, 2021

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 7, 2021

    V200 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 9, 2020

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 21, 2021

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 6, 2013

    OLYMPUS EVIS EXERA SIGMOIDOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code FDS·May 19, 2011

    BIPOL LEAD MODEL 300

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·August 6, 2008