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

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    RS-3000 ADVANCE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HHM

    FDA UDI
    Oticon A/S·05707131258793·H150, MINIRITE 312 WL CNB HHM

    Phantom® Fibula Nail System

    FDA UDI
    Paragon 28, Inc.·00889795137159·2.3mm x 230mm, Sterilization K-Wire Container

    BROTHERS POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CERVICAL STANDALONE INTERVERTEBRAL BODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 4, 2024

    CD HORIZON BALLAST SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NKB·December 9, 2019

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code LIX·May 1, 2013

    TPS HANDPIECE CORD

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZI·June 11, 2011

    INTEGRIS ALLURA 15 - 12

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code IZI·August 20, 2008