BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    GLOVE, SUPERFLEX MOLDED

    FDA 510(k)
    FDA Class 1 ·Radiology

    VerSys®

    FDA UDI
    Zimmer, Inc.·00889024362154·

    TRULY AUTOMATIC BLOOD PRESSURE MONITOR, MODEL DB11

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Percuvance Percutaneous Surgical System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    32MM +4 LFIT V40 HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·January 9, 2018

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·April 30, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 28, 2007

    POWERED PATIENT ROTATION BED

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code IKZ·October 11, 2012

    Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);

    FDA Enforcement
    Class I ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025