BEUDAMED
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    FDA UDI
    NIHON KOHDEN AMERICA, INC.·00841983103711·HL-7 NEUROWORKBENCH INTERFACE

    NA

    FDA UDI
    NIHON KOHDEN AMERICA, INC.·00841983103636·HL-7 INTERFACE FOR NEUROWORKBENCH SOFTWARE

    UNK - CONSTRUCTS: RAFN

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HSB·September 23, 2022

    NEUROMASTER

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code GWF·April 9, 2025

    UNKNOWN ALPHA RETROGRADE NAIL

    FDA Adverse Event
    Injury ·STRYKER TRAUMA KIEL·Product code HSB·January 17, 2023

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·August 5, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·August 5, 2014

    NI

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code OLT·February 20, 2021

    UNK - CONSTRUCTS: EXPERT TIBIAL NAIL

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code JDS·March 29, 2021

    MEDTRONIC PIGTAIL CARDIAC CASCADE UHF NWB

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL, INC.·Product code DQO·December 10, 1996

    5.0MM TI LOCKING SCREW SELF-DRILLING

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·September 28, 2006

    GUARDIAN

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES LP·Product code IPR·October 14, 2022

    UNK

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·January 17, 2003

    4.5MM LCP CONDYLAR PLATE 8 HOLES/206MM-RIGHT

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HRS·August 1, 2008

    VISERA CYSTO-NEPHRO VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FAJ·September 1, 2017

    NEUROFAX

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code OLT·May 9, 2024

    EVOKED RESPONSE ELECTRIC STIMULATOR

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code GWF·February 8, 2024

    NI

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code OLT·February 20, 2021

    CORETECH ROM KNEE IMOBILIZER

    FDA Adverse Event
    Injury ·VIVE HEALTH LLC·Product code ITQ·November 14, 2025

    4.5MM LCP CONDYLAR PLATE 8 HOLES/206MM-LEFT

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HRS·August 26, 2010