BEUDAMED
    10 results · 26ms · Sources: EU EUDAMED, US FDA

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    OXICOMPLUS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PAQ.112X100X300.ELAN1100

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763008668·

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930791120700·7 French Suction Tube

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0112070·Tap, Cannulated, 5.5 mm

    SYRINGE 50ML LL CLEAR 14GA 1-1/4IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·January 14, 2021

    LASER PERIPHERALS REUSABLE HOLMIUM FIBER

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

    RESPIRE BLUE SERIES

    FDA 510(k)
    FDA Class 2 ·Dental

    COLLEAGUE CXE VOLUMETRICINFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 30, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 2, 2014

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 10, 2012