BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Orthoscan Tau Mini C-Arm

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATION TO NANMA VACUUM PUMP

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ENDOSSEOUS DENTAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Dental

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·October 23, 2008

    ION PACLITAXEL-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·August 16, 2011

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·GUIDANT PUERTO RICO BV·Product code NVY·July 9, 2013

    BD LUER-LOK SYRINGE STERILE, SINGLE USE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 7, 2021

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 7, 2014

    DRX Revolution Mobile X-Ray System

    FDA Enforcement
    Class II ·Ongoing·Carestream Health, Inc.·December 13, 2023