BEUDAMED
    24 results · 29ms · Sources: EU EUDAMED, US FDA

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    NES Reprocessed RF Stylet (RFS)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526550193·GENUMEDI PT KNEE SUP SILVER R EW IV

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814770·GENUMEDI EXTRA WIDE SILVER SIZE IV

    CENTRONAIL TITANIUM UNIVERSAL FEMORAL NAILING SYSTEM

    FDA UDI
    ORTHOFIX SRL·18032568039634·RADIOLUCENT DRILL GUIDE D. 10/4.8 MM L. 165 MM

    M3810A PHILIPS TELEMONITORING SYSTEM WITH EDEVICE BRIDGED130

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DUOWEDGE SYNTHETIC BONE SUBSTITUTE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPTICROSS HD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·March 28, 2025

    OPTICROSS? HD

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·July 7, 2025

    OPTICROSS? HD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·July 22, 2025

    OPTICROSS? HD

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·February 11, 2025

    OPTICROSS? HD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·April 3, 2025

    OPTICROSS? HD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·December 11, 2025

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 26, 2023

    OPTICROSS? HD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·September 16, 2025

    OPTICROSS? HD

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·January 13, 2026

    ITOTAL TIBIAL TRAY IMPACTOR TIP

    FDA Adverse Event
    Malfunction ·CONFORMIS·Product code LXH·May 31, 2013

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 23, 2011

    GE OEC 9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC·Product code JAA·September 19, 2008

    OPTICROSS? HD

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·May 22, 2025

    OPTICROSS? HD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OBJ·February 26, 2025