BEUDAMED
    16 results · 18ms · Sources: EU EUDAMED, US FDA

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    CR5 CARDIAC MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209112180·KIT, INDIVIDUAL BLEEDING CONTROL - (vac) - CUSTOM

    Crosperio RX PTA Balloon Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURFLO WINGED INFUSION SET WITH NEEDLE PROTECTION (SURSHIELD), MODEL SV-S23BL35VS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DELTA CER HEAD 12/14 36MM +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LZO·February 2, 2026

    SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·June 4, 2019

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 6, 2014

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·November 30, 2012

    LASIK

    FDA Adverse Event
    Injury ·Product code LZS·September 29, 2010

    SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·March 1, 2024

    SHIDEN

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 10, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·April 18, 2022

    SHIDEN

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 2, 2021

    SHIDEN

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·January 6, 2022