BEUDAMED
    10 results · 31ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    FUSION DIGITAL DIAGNOSTIC X-RAY UPGRADE KIT

    FDA 510(k)
    FDA Class 2 ·Radiology

    Biomet® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304001367·

    ACON TRI-FECT DRUG SCREEN TEST DEVICE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    5MM FLARED CANNULA MODEL 420262, 8MM FLARED CANNULA MODEL 420319

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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 29, 2026

    BD INTIMA-II 20GAX1.16IN PRN SLM NPVC

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code FOZ·January 13, 2022

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·October 4, 2014

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    VANGUARD SSK DIRECT COMPRESSION MOLDED POLYETHYLENE CONSTRAINED TIBIAL BEARING 1

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 12, 2016