BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    BENACEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    Amara View

    FDA UDI
    Respironics, Inc.·00606959009165·Amara View Mask without Headgear, Small

    Tiche PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481476927·

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0106120·Trial, 26 x 12mm, 8 Degree, Tapered, Straight

    VECTORVISION KNEE

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE

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

    Star 60

    FDA UDI
    SKANRAY TECHNOLOGIES LIMITED·18904269450769·Multipara Patient monitoring system

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 17, 2025

    NUCLEUS 24 AUDITORY BRAINSTEM IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD .·Product code MCM·May 2, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·September 15, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 26, 2011

    INFANT DUAL-HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BZE·March 18, 2010

    INFANT BIAS FLOW BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·December 7, 2010

    RESPIRATORY HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·November 15, 2011