BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    MARZ-175

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    LM-Dental 811199

    Device
    EU MDR · Eu Md Class 1 ·LM-Instruments Oy·Not intended for eu market

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·May 7, 2021

    PROVIEW EYE PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM 3.4MM IMPLANT ANGLED ABUTMENTS

    FDA 510(k)
    FDA Class 2 ·Dental

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 9, 2014

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012

    DUROM US ACETABULAR COMPONENT 56/50 P

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code KXA·August 10, 2010

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·June 13, 2019

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·February 27, 2019

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·July 14, 2023

    DRIVING CAP/THREADED

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·July 24, 2025