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

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    Vacutore Air/Water Bottle Tubing

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

    Speedlock

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657044851·Metzenbaum, 5mm, Straight, Serrated Handle: 136...

    I-LIPO, MODELS A00-1238 (230V), A00-1239 (120V)

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

    INSUFLOW DEWHEART

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·December 20, 2018

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·May 2, 2025

    UPHOLD VAGINAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 26, 2013

    TRAUMA STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·July 28, 2011

    SOMATOM DEFINITION

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code JAK·September 26, 2008

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·April 1, 2019

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·March 8, 2018