BEUDAMED
    315 results · 17ms · Sources: EU EUDAMED, US FDA

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    XIA 3 TITANIUM BLOCKER

    FDA Adverse Event
    Injury ·STRYKER SPINE-US·Product code NKB·April 3, 2025

    XIA 3 TITANIUM BLOCKER

    FDA Adverse Event
    Injury ·STRYKER SPINE-US·Product code NKB·April 3, 2025

    XIA 3 TITANIUM BLOCKER

    FDA Adverse Event
    Injury ·STRYKER SPINE-US·Product code NKB·April 3, 2025

    TALENT AAA STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·April 18, 2017

    ANEURX

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·April 18, 2017

    ENDURANT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·April 18, 2017

    Lens, Fresnel, Flexible, Diagnostic

    FDA classification
    FDA Class 1 ·Lens, Fresnel, Flexible, Diagnostic

    HJ® 3tlg. 20ML LL

    FDA UDI
    Henke-Sass, Wolf GmbH·04035873063131·HSW HENKE-JECT® 3-TLG. 20 ML LL

    SJJ

    FDA UDI
    PROSUM MEDICAL LIMITED·15056093011227·Small Volume Syringe 0.2ml Luer Lock with Cap a...

    Galeo Pro

    FDA UDI
    CONCERT MEDICAL, LLC·00814384020277·Coronary Guidewire

    HJY SMART MEDICAL DEVICE CO., LTD.

    FDA registration
    HJY SMART MEDICAL DEVICE CO., LTD.·3 products·🇹🇼 Taiwan

    Thermo Scientific

    FDA UDI
    RICHARD-ALLAN SCIENTIFIC COMPANY·00673693404877·UltraVision ONE Detection System HRP Polymer (R...

    Subdural Electrode

    FDA UDI
    Ad-Tech Medical Instrument Corporation·00841823101549·

    HJD CALCAR REPLACEMENT PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HJY VisualNext Endoscopic Vision System

    FDA 510(k)
    FDA Class 2 ·Neurology

    MODULAR COLLARED HJD TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RESUBMITTING OF HJD TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HJY VisualNext 3D Endoscopic Vision System

    FDA 510(k)
    FDA Class 2 ·Neurology

    JOHNSON & JOHNSON CORDIS

    FDA Adverse Event
    Injury ·*·Product code MAF·December 11, 1997

    HJD TOTAL HIP SYSTEM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC. ORTHOPAEDICS DIV.·Product code KWY·July 24, 1998