BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    NOBLUS™ Ultrasound Diagnostic System

    FDA 510(k)
    FDA Class 2 ·Radiology

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970355·

    ZOLL R SERIES DEFIBRILLATOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    MYOSURE HYSTEROSCOPIC TISSUE REMOVAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BD BACTEC PLUS AEROBIC/F CULTURE VIALS (PLASTIC)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code MDB·October 4, 2021

    ENTRUST ESCUDO VR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWS·June 10, 2013

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·July 6, 2011

    PROTECTA XT CRT-D

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014