BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    Restrata®

    FDA 510(k)
    FDA Unclassified ·Unknown

    DC-7 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    EP -NURSEMATE, EP -NURSEMATE WITH PHYSIO MODULE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PLUM XL PLS MIC/MAC

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 14, 2011

    2.4MM VA LOCKING SCREW STARDRIVE 20MM

    FDA Adverse Event
    Injury ·SYNTHESF (USA)·Product code HWC·June 27, 2013

    PROTEGE RX SELF EXPANDING NITINOL STENT

    FDA Adverse Event
    Injury ·EV3 INC.·Product code FGE·September 29, 2008

    NV EHXL ALIP LNR G4 36MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 18, 2022

    SENSOR MMT-7040A GUARDIAN4 5PK US

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 19, 2025