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

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    HIP FRACTURE STEM FENESTRATION PLUG

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    T2 - NAIL HOLDING SCREW, TIBIA 10 MM

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·May 21, 2025

    T2 - NAIL HOLDING SCREW, TIBIA 10 MM

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·June 23, 2025

    FIAX TEST KIT FOR MEASLES-G ANTIBODIES FLYORESCENT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Tubli-Seal, Tubli-Seal EWT,Tubli-Seal Xpress, Tubli-Seal EWT Xpress

    FDA 510(k)
    FDA Class 2 ·Dental

    APPLIANCE, FIXATION DEVICE, PROXIMAL FEMUR

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDO·November 13, 2014

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·February 9, 2013

    MARQUIS DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code LWS·January 7, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 23, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 13, 2014

    T2 - NAIL HANDLE

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·May 21, 2025