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

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    LEEP SYSTEM 1000

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

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150669·K-WIRE - SINGLE TROCAR THREADED 2.4mm DIA x 200mm

    3M™ Victory Series™

    FDA UDI
    3M UNITEK CORPORATION·00652221116215·3M™ Victory Series™ First Molar Bands, 952-483,...

    Digital Automatic Blood Pressure Monitor BPM30 and BPM31 Series

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNTHES (USA) SPHERICAL WASHERS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TERUMO CAPIOX FX 25

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS·Product code DTZ·June 5, 2014

    VIRTUOSO VR

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LWS·February 9, 2013

    CRE BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·January 7, 2011

    ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020