BEUDAMED
    12 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Synxess Neurovascular Guidewire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AXERA 2 ACCESS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FACEMASTER FACIAL TONING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    GLIDEWELL HT IMPLANT Ø4.3 X 10 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·May 14, 2025

    GLIDEWELL HT IMPLANT Ø4.3 X 10 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·April 4, 2025

    GLIDEWELL HT IMPLANT Ø4.3 X 10 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·June 20, 2025

    GLIDEWELL HT IMPLANT Ø4.3 X 10 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·January 29, 2026

    IMMULITE 2000 TOXOPLASMA IGG

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code LGD·November 6, 2008

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP.·Product code DRY·August 16, 2011

    FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·July 22, 2013

    Femoral Head

    FDA UDI
    FOURNITURES HOSPITALIERES INDUSTRIE·03661489408717·

    BD LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMF·April 25, 2019