BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    MANUAL PULMONARY RESUSICITATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ZAVATION

    FDA UDI
    Zavation LLC·00842166117235·Polyaxial Screw 3.5mm x 46mm

    PINK CAD/CAM disc

    FDA 510(k)
    FDA Class 2 ·Dental

    SONICATOR 740, MODEL ME 740

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    2.8MM DRILL BIT/QC/165MM

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HTW·July 9, 2019

    SPRINT QUATTRO

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·February 9, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·January 5, 2011

    AIM-ARM F/A2FN

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code LXH·July 23, 2014

    1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015