BEUDAMED
    9 results · 25ms · Sources: EU EUDAMED, US FDA

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    Responsive Arthroscopy Suture Anchor System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    19-INCH (48CM) 1.3M COLOR LCD MONITOR CDL1909A

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDTOX BUPRENORPHINE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 17, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 20, 2013

    TRANSSEPTAL NEEDLE, XS, BRK-1, 71CM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, AF DIVISION·Product code DRC·July 7, 2011

    EXPORT AP ASPIRATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC, INC·Product code DXE·January 28, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·April 19, 2019

    EXPORT AP ASPIRATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC, INC·Product code DXE·March 27, 2019