BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    STATUS FIRST STREP A

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Plateau-LO Spacer System

    FDA UDI
    Life Spine, Inc.·00190837027834·PLATEAU-LO Interbody, 10mm x 40mm x 8mm, 7°

    APPLICATOR TIP/DUAL SPRAYER KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PHILIPS PAGEWRITER TOUCH CARDIOGRAPH, MODEL M5000A SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VISION HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·GISH BIOMEDICAL, INC.·Product code DTZ·February 18, 2011

    VISERA ELITE II VIDEO SYSTEM CENTER

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·October 16, 2023

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 8, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 27, 2014

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 6, 2011

    OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE -Absorbable Suture anchor Product Number: 72201995

    FDA Enforcement
    Class II ·Ongoing·Smith & Nephew, Inc.·October 28, 2020